Canonical Allele Identifier: CA16040854
Gene: NEB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 370296
ClinVar RCV Id: RCV000411004
dbSNP Id: rs1057516381

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.151674585C>A , CM000664.2:g.151674585C>A GRCh38
NC_000002.11:g.152531099C>A , CM000664.1:g.152531099C>A GRCh37
NC_000002.10:g.152239345C>A NCBI36
NG_009382.2:g.64903G>T , LRG_202:g.64903G>T

Transcript Alleles

HGVS Amino-acid change
NM_001164507.1:c.3880-1G>T VV NP_001157979.1:p.=
NM_001164508.1:c.3880-1G>T VV NP_001157980.1:p.=
NM_001271208.1:c.3880-1G>T , LRG_202t1:c.3880-1G>T NP_001258137.1:p.=
NM_004543.4:c.3880-1G>T VV NP_004534.2:p.=
XM_005246590.1:c.3880-1G>T XP_005246647.1:p.=
XM_005246591.1:c.3880-1G>T XP_005246648.1:p.=
XM_005246592.1:c.3880-1G>T XP_005246649.1:p.=
XM_005246593.1:c.3880-1G>T XP_005246650.1:p.=
XM_005246594.1:c.3880-1G>T XP_005246651.1:p.=
XM_005246595.1:c.3880-1G>T XP_005246652.1:p.=
XM_005246596.1:c.3880-1G>T XP_005246653.1:p.=
XM_005246597.1:c.3880-1G>T XP_005246654.1:p.=
XM_005246598.1:c.3880-1G>T XP_005246655.1:p.=
XM_005246599.1:c.3880-1G>T XP_005246656.1:p.=
XM_005246600.1:c.3880-1G>T XP_005246657.1:p.=
XM_005246601.1:c.3880-1G>T XP_005246658.1:p.=
XM_005246602.1:c.3880-1G>T XP_005246659.1:p.=
XM_005246603.1:c.3880-1G>T XP_005246660.1:p.=
XM_005246604.1:c.3880-1G>T XP_005246661.1:p.=
XM_005246606.1:c.3880-1G>T XP_005246663.1:p.=
XM_005246608.1:c.3880-1G>T XP_005246665.1:p.=
XM_005246610.1:c.3880-1G>T XP_005246667.1:p.=
XM_005246611.1:c.3880-1G>T XP_005246668.1:p.=
XM_005246612.1:c.3880-1G>T XP_005246669.1:p.=
XM_005246613.1:c.3880-1G>T XP_005246670.1:p.=
XM_005246615.1:c.3880-1G>T XP_005246672.1:p.=
XM_005246616.1:c.3880-1G>T XP_005246673.1:p.=
XM_005246617.1:c.3880-1G>T XP_005246674.1:p.=
XM_006712541.1:c.3880-1G>T XP_006712604.1:p.=
XM_006712542.1:c.3880-1G>T XP_006712605.1:p.=
XM_011511224.1:c.3880-1G>T XP_011509526.1:p.=
XM_011511225.1:c.3880-1G>T XP_011509527.1:p.=
XM_011511226.1:c.3880-1G>T XP_011509528.1:p.=
XM_011511227.1:c.3880-1G>T XP_011509529.1:p.=
XM_005246590.2:c.3880-1G>T
XM_005246591.2:c.3880-1G>T
XM_005246592.2:c.3880-1G>T
XM_005246593.2:c.3880-1G>T
XM_005246594.2:c.3880-1G>T
XM_005246596.2:c.3880-1G>T
XM_005246597.2:c.3880-1G>T
XM_005246598.2:c.3880-1G>T
XM_005246599.2:c.3880-1G>T
XM_005246601.2:c.3880-1G>T
XM_005246602.2:c.3880-1G>T
XM_005246603.2:c.3880-1G>T
XM_005246604.2:c.3880-1G>T
XM_005246606.2:c.3880-1G>T
XM_005246608.2:c.3880-1G>T
XM_005246610.2:c.3880-1G>T
XM_005246611.2:c.3880-1G>T
XM_005246612.2:c.3880-1G>T
XM_005246613.2:c.3880-1G>T
XM_005246615.2:c.3880-1G>T
XM_005246617.2:c.3880-1G>T
XM_006712541.2:c.3880-1G>T
XM_006712542.2:c.3880-1G>T
XM_011511225.2:c.3880-1G>T
XM_011511226.2:c.3880-1G>T
XM_011511227.2:c.3880-1G>T
XM_017004177.1:c.3880-1G>T XP_016859666.1:p.=
XM_017004178.1:c.3880-1G>T XP_016859667.1:p.=
XM_017004179.1:c.3880-1G>T XP_016859668.1:p.=
XM_017004180.1:c.3880-1G>T XP_016859669.1:p.=
XM_017004181.1:c.3880-1G>T XP_016859670.1:p.=
XM_017004182.1:c.3880-1G>T XP_016859671.1:p.=
XM_017004183.1:c.3880-1G>T XP_016859672.1:p.=
XM_017004184.1:c.3880-1G>T XP_016859673.1:p.=
XM_017004185.1:c.3880-1G>T XP_016859674.1:p.=
NM_001271208.2:c.3880-1G>T VV NP_001258137.2:p.=
ENST00000172853.14:c.3880-1G>T ENSP00000172853.10:p.=
ENST00000397345.7:c.3880-1G>T ENSP00000380505.3:p.=
ENST00000409198.5:c.3880-1G>T ENSP00000386259.1:p.=
ENST00000427231.6:c.3880-1G>T ENSP00000416578.2:p.=
ENST00000603639.5:n.3880-1G>T ENSP00000473894.1:p.=
ENST00000604864.5:n.3880-1G>T ENSP00000474498.1:p.=
ENST00000618972.4:c.3880-1G>T ENSP00000484342.1:p.=