Canonical Allele Identifier: CA2561329102
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31354810-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354810A>T , CM000668.2:g.31354810A>T GRCh38
NC_000006.11:g.31322587A>T , CM000668.1:g.31322587A>T GRCh37
NC_000006.10:g.31430566A>T NCBI36
NG_023187.1:g.7403T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3060-145T>A
ENST00000481849.6:n.2875T>A
ENST00000497377.6:n.2782T>A
ENST00000640094.2:c.896-145T>A ENSP00000491275.2:n.896-145T>A
ENST00000696558.1:c.1082-145T>A ENSP00000512716.1:n.1082-145T>A
ENST00000696559.1:c.1013-145T>A ENSP00000512717.1:n.1013-145T>A
ENST00000696560.1:c.1013-145T>A ENSP00000512718.1:n.1013-145T>A
ENST00000696561.1:c.1013-145T>A ENSP00000512719.1:n.1013-145T>A
ENST00000696562.1:c.1013-145T>A ENSP00000512720.1:n.1013-145T>A
ENST00000412585.7:c.1013-145T>A MANE Select ENSP00000399168.2:n.1013-145T>A
ENST00000640094.1:c.89-145T>A ENSP00000491275.1:n.89-145T>A
ENST00000412585.6:c.1013-145T>A ENSP00000399168.2:n.1013-145T>A
ENST00000497377.5:n.267T>A
NM_005514.6:c.1013-145T>A NP_005505.2:n.1013-145T>A
XM_011514556.1:c.1046-145T>A XP_011512858.1:n.1046-145T>A
XM_011514557.1:c.896-145T>A XP_011512859.1:n.896-145T>A
XR_926175.1:n.1452-145T>A
NM_005514.7:c.1013-145T>A NP_005505.2:n.1013-145T>A
NM_005514.8:c.1013-145T>A MANE Select NP_005505.2:n.1013-145T>A