Canonical Allele Identifier: CA136832911
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341351
gnomAD v4: 6-31355493-G-A
MyVariant Identifiers: chr6:g.31323270G>A (hg19) chr6:g.31355493G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355493G>A , CM000668.2:g.31355493G>A GRCh38
NC_000006.11:g.31323270G>A , CM000668.1:g.31323270G>A GRCh37
NC_000006.10:g.31431249G>A NCBI36
NG_023187.1:g.6720C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2766C>T
ENST00000481849.6:n.2192C>T
ENST00000497377.6:n.2192C>T
ENST00000640094.2:c.719C>T ENSP00000491275.2:p.Thr240Ile
ENST00000696558.1:c.788C>T ENSP00000512716.1:n.788C>T
ENST00000696559.1:c.719C>T ENSP00000512717.1:p.Thr240Ile
ENST00000696560.1:c.719C>T ENSP00000512718.1:p.Thr240Ile
ENST00000696561.1:c.719C>T ENSP00000512719.1:p.Thr240Ile
ENST00000696562.1:c.719C>T ENSP00000512720.1:p.Thr240Ile
ENST00000412585.7:c.719C>T MANE Select ENSP00000399168.2:p.Thr240Ile
ENST00000412585.6:c.719C>T ENSP00000399168.2:p.Thr240Ile
ENST00000463574.1:n.310C>T
ENST00000498007.1:n.985C>T
NM_005514.6:c.719C>T NP_005505.2:p.Thr240Ile
XM_011514556.1:c.752C>T XP_011512858.1:p.Thr251Ile
XM_011514557.1:c.719C>T XP_011512859.1:p.Thr240Ile
XR_926175.1:n.1158C>T
NM_005514.7:c.719C>T NP_005505.2:p.Thr240Ile
NM_005514.8:c.719C>T MANE Select NP_005505.2:p.Thr240Ile
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