Canonical Allele Identifier: CA1619119750
Gene: HLA-B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355948T>A , CM000668.2:g.31355948T>A GRCh38
NC_000006.11:g.31323725T>A , CM000668.1:g.31323725T>A GRCh37
NC_000006.10:g.31431704T>A NCBI36
NG_023187.1:g.6265A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2311A>T
ENST00000481849.6:n.2092+219A>T
ENST00000497377.6:n.2092+219A>T
ENST00000640094.2:c.619+219A>T ENSP00000491275.2:n.619+219A>T
ENST00000696558.1:c.620-142A>T ENSP00000512716.1:n.620-142A>T
ENST00000696559.1:c.619+219A>T ENSP00000512717.1:n.619+219A>T
ENST00000696560.1:c.619+219A>T ENSP00000512718.1:n.619+219A>T
ENST00000696561.1:c.619+219A>T ENSP00000512719.1:n.619+219A>T
ENST00000696562.1:c.619+219A>T ENSP00000512720.1:n.619+219A>T
ENST00000412585.7:c.619+219A>T MANE Select ENSP00000399168.2:n.619+219A>T
ENST00000412585.6:c.619+219A>T ENSP00000399168.2:n.619+219A>T
ENST00000434333.1:c.652+219A>T ENSP00000405931.1:n.652+219A>T
ENST00000474381.1:n.713A>T
ENST00000498007.1:n.885+219A>T
NM_005514.6:c.619+219A>T NP_005505.2:n.619+219A>T
XM_011514556.1:c.652+219A>T XP_011512858.1:n.652+219A>T
XM_011514557.1:c.619+219A>T XP_011512859.1:n.619+219A>T
XR_926175.1:n.848A>T
NM_005514.7:c.619+219A>T NP_005505.2:n.619+219A>T
NM_005514.8:c.619+219A>T MANE Select NP_005505.2:n.619+219A>T
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