Canonical Allele Identifier: CA2677952945
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31354050-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354050G>T , CM000668.2:g.31354050G>T GRCh38
NC_000006.11:g.31321827G>T , CM000668.1:g.31321827G>T GRCh37
NC_000006.10:g.31429806G>T NCBI36
NG_023187.1:g.8163C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3387C>A
ENST00000481849.6:n.3347C>A
ENST00000497377.6:n.3254C>A
ENST00000696558.1:c.1409C>A ENSP00000512716.1:n.1409C>A
ENST00000696559.1:c.*251C>A ENSP00000512717.1:n.*251C>A
ENST00000696560.1:c.*251C>A ENSP00000512718.1:n.*251C>A
ENST00000696561.1:c.*251C>A ENSP00000512719.1:n.*251C>A
ENST00000696562.1:c.*251C>A ENSP00000512720.1:n.*251C>A
ENST00000412585.7:c.*251C>A MANE Select ENSP00000399168.2:n.*251C>A
ENST00000412585.6:c.*251C>A ENSP00000399168.2:n.*251C>A
ENST00000481849.5:n.575C>A
ENST00000497377.5:n.739C>A
NM_005514.6:c.*251C>A NP_005505.2:n.*251C>A
XM_011514556.1:c.*251C>A XP_011512858.1:n.*251C>A
XM_011514557.1:c.*251C>A XP_011512859.1:n.*251C>A
XR_926175.1:n.1779C>A
NM_005514.7:c.*251C>A NP_005505.2:n.*251C>A
NM_005514.8:c.*251C>A MANE Select NP_005505.2:n.*251C>A
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