Canonical Allele Identifier: CA3711283
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs76503987
gnomAD v2: 6-31322986-A-G
gnomAD v3: 6-31355209-A-G
gnomAD v4: 6-31355209-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355209A>G , CM000668.2:g.31355209A>G GRCh38
NC_000006.11:g.31322986A>G , CM000668.1:g.31322986A>G GRCh37
NC_000006.10:g.31430965A>G NCBI36
NG_023187.1:g.7004T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2957T>C
ENST00000481849.6:n.2476T>C
ENST00000497377.6:n.2383T>C
ENST00000640094.2:c.895+108T>C ENSP00000491275.2:n.895+108T>C
ENST00000696558.1:c.979T>C ENSP00000512716.1:n.979T>C
ENST00000696559.1:c.910T>C ENSP00000512717.1:p.Ser304Pro
ENST00000696560.1:c.910T>C ENSP00000512718.1:p.Ser304Pro
ENST00000696561.1:c.910T>C ENSP00000512719.1:p.Ser304Pro
ENST00000696562.1:c.910T>C ENSP00000512720.1:p.Ser304Pro
ENST00000412585.7:c.910T>C MANE Select ENSP00000399168.2:p.Ser304Pro
ENST00000640094.1:c.88+108T>C ENSP00000491275.1:n.88+108T>C
ENST00000412585.6:c.910T>C ENSP00000399168.2:p.Ser304Pro
ENST00000463574.1:n.501T>C
NM_005514.6:c.910T>C NP_005505.2:p.Ser304Pro
XM_011514556.1:c.943T>C XP_011512858.1:p.Ser315Pro
XM_011514557.1:c.895+108T>C XP_011512859.1:n.895+108T>C
XR_926175.1:n.1349T>C
NM_005514.7:c.910T>C NP_005505.2:p.Ser304Pro
NM_005514.8:c.910T>C MANE Select NP_005505.2:p.Ser304Pro