Canonical Allele Identifier: CA175326088
Gene: NRG1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10093107

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.32168933C>T , CM000670.2:g.32168933C>T GRCh38
NC_000008.10:g.32026449C>T , CM000670.1:g.32026449C>T GRCh37
NC_000008.9:g.32145991C>T NCBI36
NG_012005.1:g.534182C>T
NG_012005.2:g.534712C>T

Transcript Alleles

HGVS Amino-acid change
NM_001159995.1:c.38-426895C>T VV NP_001153467.1:p.=
NM_001159999.1:c.38-426895C>T VV NP_001153471.1:p.=
NM_001160001.1:c.38-426895C>T VV NP_001153473.1:p.=
NM_013962.2:c.746-426895C>T VV NP_039256.2:p.=
XM_011544512.1:c.122-426895C>T XP_011542814.1:p.=
NM_001159995.2:c.38-426895C>T VV
NM_001159999.2:c.38-426895C>T VV
NM_001160001.2:c.38-426895C>T VV
NM_001322201.1:c.-555-426895C>T VV NP_001309130.1:p.=
NM_001322202.1:c.-504-426895C>T VV NP_001309131.1:p.=
XM_011544512.2:c.122-426895C>T
XM_017013365.2:c.122-426895C>T XP_016868854.1:p.=
XM_017013366.2:c.122-426895C>T XP_016868855.1:p.=
XM_017013367.1:c.122-426895C>T XP_016868856.1:p.=
XM_017013371.2:c.122-426895C>T XP_016868860.1:p.=
XM_017013372.2:c.122-426895C>T XP_016868861.1:p.=
ENST00000518104.5:c.38-426895C>T ENSP00000430053.1:p.=
ENST00000519301.5:c.38-426895C>T ENSP00000429582.1:p.=
ENST00000520407.5:c.746-426895C>T ENSP00000434640.1:p.=
ENST00000523534.5:n.305-426895C>T ENSP00000429067.1:p.=