Canonical Allele Identifier: CA3711329
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs41541515
gnomAD v2: 6-31323115-T-C
gnomAD v3: 6-31355338-T-C
gnomAD v4: 6-31355338-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355338T>C , CM000668.2:g.31355338T>C GRCh38
NC_000006.11:g.31323115T>C , CM000668.1:g.31323115T>C GRCh37
NC_000006.10:g.31431094T>C NCBI36
NG_023187.1:g.6875A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2921A>G
ENST00000481849.6:n.2347A>G
ENST00000497377.6:n.2347A>G
ENST00000640094.2:c.874A>G ENSP00000491275.2:p.Lys292Glu
ENST00000696558.1:c.943A>G ENSP00000512716.1:n.943A>G
ENST00000696559.1:c.874A>G ENSP00000512717.1:p.Lys292Glu
ENST00000696560.1:c.874A>G ENSP00000512718.1:p.Lys292Glu
ENST00000696561.1:c.874A>G ENSP00000512719.1:p.Lys292Glu
ENST00000696562.1:c.874A>G ENSP00000512720.1:p.Lys292Glu
ENST00000412585.7:c.874A>G MANE Select ENSP00000399168.2:p.Lys292Glu
ENST00000640094.1:c.67A>G ENSP00000491275.1:p.Lys23Glu
ENST00000412585.6:c.874A>G ENSP00000399168.2:p.Lys292Glu
ENST00000463574.1:n.465A>G
NM_005514.6:c.874A>G NP_005505.2:p.Lys292Glu
XM_011514556.1:c.907A>G XP_011512858.1:p.Lys303Glu
XM_011514557.1:c.874A>G XP_011512859.1:p.Lys292Glu
XR_926175.1:n.1313A>G
NM_005514.7:c.874A>G NP_005505.2:p.Lys292Glu
NM_005514.8:c.874A>G MANE Select NP_005505.2:p.Lys292Glu