Canonical Allele Identifier: CA136832028
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341395
gnomAD v3: 6-31354676-A-C
gnomAD v4: 6-31354676-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354676A>C , CM000668.2:g.31354676A>C GRCh38
NC_000006.11:g.31322453A>C , CM000668.1:g.31322453A>C GRCh37
NC_000006.10:g.31430432A>C NCBI36
NG_023187.1:g.7537T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3060-11T>G
ENST00000481849.6:n.3009T>G
ENST00000497377.6:n.2916T>G
ENST00000640094.2:c.896-11T>G ENSP00000491275.2:n.896-11T>G
ENST00000696558.1:c.1082-11T>G ENSP00000512716.1:n.1082-11T>G
ENST00000696559.1:c.1013-11T>G ENSP00000512717.1:n.1013-11T>G
ENST00000696560.1:c.1013-11T>G ENSP00000512718.1:n.1013-11T>G
ENST00000696561.1:c.1013-11T>G ENSP00000512719.1:n.1013-11T>G
ENST00000696562.1:c.1013-11T>G ENSP00000512720.1:n.1013-11T>G
ENST00000412585.7:c.1013-11T>G MANE Select ENSP00000399168.2:n.1013-11T>G
ENST00000640094.1:c.89-11T>G ENSP00000491275.1:n.89-11T>G
ENST00000412585.6:c.1013-11T>G ENSP00000399168.2:n.1013-11T>G
ENST00000481849.5:n.131T>G
ENST00000497377.5:n.401T>G
NM_005514.6:c.1013-11T>G NP_005505.2:n.1013-11T>G
XM_011514556.1:c.1046-11T>G XP_011512858.1:n.1046-11T>G
XM_011514557.1:c.896-11T>G XP_011512859.1:n.896-11T>G
XR_926175.1:n.1452-11T>G
NM_005514.7:c.1013-11T>G NP_005505.2:n.1013-11T>G
NM_005514.8:c.1013-11T>G MANE Select NP_005505.2:n.1013-11T>G