Canonical Allele Identifier: CA136832464
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs41550414
gnomAD v4: 6-31355161-C-T
MyVariant Identifiers: chr6:g.31322938C>T (hg19) chr6:g.31355161C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355161C>T , CM000668.2:g.31355161C>T GRCh38
NC_000006.11:g.31322938C>T , CM000668.1:g.31322938C>T GRCh37
NC_000006.10:g.31430917C>T NCBI36
NG_023187.1:g.7052G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3005G>A
ENST00000481849.6:n.2524G>A
ENST00000497377.6:n.2431G>A
ENST00000640094.2:c.895+156G>A ENSP00000491275.2:n.895+156G>A
ENST00000696558.1:c.1027G>A ENSP00000512716.1:n.1027G>A
ENST00000696559.1:c.958G>A ENSP00000512717.1:p.Val320Ile
ENST00000696560.1:c.958G>A ENSP00000512718.1:p.Val320Ile
ENST00000696561.1:c.958G>A ENSP00000512719.1:p.Val320Ile
ENST00000696562.1:c.958G>A ENSP00000512720.1:p.Val320Ile
ENST00000412585.7:c.958G>A MANE Select ENSP00000399168.2:p.Val320Ile
ENST00000640094.1:c.88+156G>A ENSP00000491275.1:n.88+156G>A
ENST00000412585.6:c.958G>A ENSP00000399168.2:p.Val320Ile
ENST00000463574.1:n.549G>A
NM_005514.6:c.958G>A NP_005505.2:p.Val320Ile
XM_011514556.1:c.991G>A XP_011512858.1:p.Val331Ile
XM_011514557.1:c.895+156G>A XP_011512859.1:n.895+156G>A
XR_926175.1:n.1397G>A
NM_005514.7:c.958G>A NP_005505.2:p.Val320Ile
NM_005514.8:c.958G>A MANE Select NP_005505.2:p.Val320Ile
Search 100 bp 5'
Search 100 bp 3'