Canonical Allele Identifier: CA136833276
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs45577931
gnomAD v4: 6-31355995-A-T
MyVariant Identifiers: chr6:g.31323772A>T (hg19) chr6:g.31355995A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355995A>T , CM000668.2:g.31355995A>T GRCh38
NC_000006.11:g.31323772A>T , CM000668.1:g.31323772A>T GRCh37
NC_000006.10:g.31431751A>T NCBI36
NG_023187.1:g.6218T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2264T>A
ENST00000481849.6:n.2092+172T>A
ENST00000497377.6:n.2092+172T>A
ENST00000640094.2:c.619+172T>A ENSP00000491275.2:n.619+172T>A
ENST00000696558.1:c.619+172T>A ENSP00000512716.1:n.619+172T>A
ENST00000696559.1:c.619+172T>A ENSP00000512717.1:n.619+172T>A
ENST00000696560.1:c.619+172T>A ENSP00000512718.1:n.619+172T>A
ENST00000696561.1:c.619+172T>A ENSP00000512719.1:n.619+172T>A
ENST00000696562.1:c.619+172T>A ENSP00000512720.1:n.619+172T>A
ENST00000412585.7:c.619+172T>A MANE Select ENSP00000399168.2:n.619+172T>A
ENST00000412585.6:c.619+172T>A ENSP00000399168.2:n.619+172T>A
ENST00000434333.1:c.652+172T>A ENSP00000405931.1:n.652+172T>A
ENST00000474381.1:n.666T>A
ENST00000498007.1:n.885+172T>A
NM_005514.6:c.619+172T>A NP_005505.2:n.619+172T>A
XM_011514556.1:c.652+172T>A XP_011512858.1:n.652+172T>A
XM_011514557.1:c.619+172T>A XP_011512859.1:n.619+172T>A
XR_926175.1:n.801T>A
NM_005514.7:c.619+172T>A NP_005505.2:n.619+172T>A
NM_005514.8:c.619+172T>A MANE Select NP_005505.2:n.619+172T>A
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