Canonical Allele Identifier: CA15926309
Gene: SERPINB7 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1055902

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.63805309C>T , CM000680.2:g.63805309C>T GRCh38
NC_000018.9:g.61472543C>T , CM000680.1:g.61472543C>T GRCh37
NC_000018.8:g.59623523C>T NCBI36
NG_034150.1:g.57263C>T

Transcript Alleles

HGVS Amino-acid change
NM_001040147.2:c.*674C>T VV NP_001035237.1:p.=
NM_001261830.1:c.*674C>T VV NP_001248759.1:p.=
NM_001261831.1:c.*674C>T VV NP_001248760.1:p.=
NM_003784.3:c.*674C>T VV NP_003775.1:p.=
XM_006722562.1:c.*674C>T XP_006722625.1:p.=
XM_011526236.1:c.*674C>T XP_011524538.1:p.=
XM_024451278.1:c.*674C>T XP_024307046.1:p.=
NM_003784.4:c.*674C>T VV MANE Preferred NP_003775.1:p.=
ENST00000336429.6:c.*674C>T ENSP00000337212.2:p.=
ENST00000398019.6:c.*674C>T ENSP00000381101.2:p.=
ENST00000540675.5:c.*674C>T ENSP00000444572.1:p.=
ENST00000546027.5:c.*674C>T ENSP00000444861.1:p.=