Canonical Allele Identifier: CA136832285
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs144012689
gnomAD v2: 6-31322780-T-A
gnomAD v3: 6-31355003-T-A
gnomAD v4: 6-31355003-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355003T>A , CM000668.2:g.31355003T>A GRCh38
NC_000006.11:g.31322780T>A , CM000668.1:g.31322780T>A GRCh37
NC_000006.10:g.31430759T>A NCBI36
NG_023187.1:g.7210A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3059+104A>T
ENST00000481849.6:n.2682A>T
ENST00000497377.6:n.2589A>T
ENST00000640094.2:c.895+314A>T ENSP00000491275.2:n.895+314A>T
ENST00000696558.1:c.1081+104A>T ENSP00000512716.1:n.1081+104A>T
ENST00000696559.1:c.1012+104A>T ENSP00000512717.1:n.1012+104A>T
ENST00000696560.1:c.1012+104A>T ENSP00000512718.1:n.1012+104A>T
ENST00000696561.1:c.1012+104A>T ENSP00000512719.1:n.1012+104A>T
ENST00000696562.1:c.1012+104A>T ENSP00000512720.1:n.1012+104A>T
ENST00000412585.7:c.1012+104A>T MANE Select ENSP00000399168.2:n.1012+104A>T
ENST00000640094.1:c.88+314A>T ENSP00000491275.1:n.88+314A>T
ENST00000412585.6:c.1012+104A>T ENSP00000399168.2:n.1012+104A>T
ENST00000497377.5:n.74A>T
NM_005514.6:c.1012+104A>T NP_005505.2:n.1012+104A>T
XM_011514556.1:c.1045+104A>T XP_011512858.1:n.1045+104A>T
XM_011514557.1:c.895+314A>T XP_011512859.1:n.895+314A>T
XR_926175.1:n.1451+104A>T
NM_005514.7:c.1012+104A>T NP_005505.2:n.1012+104A>T
NM_005514.8:c.1012+104A>T MANE Select NP_005505.2:n.1012+104A>T