Canonical Allele Identifier: CA2581562230
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31354145-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354145G>T , CM000668.2:g.31354145G>T GRCh38
NC_000006.11:g.31321922G>T , CM000668.1:g.31321922G>T GRCh37
NC_000006.10:g.31429901G>T NCBI36
NG_023187.1:g.8068C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3292C>A
ENST00000481849.6:n.3252C>A
ENST00000497377.6:n.3159C>A
ENST00000696558.1:c.1314C>A ENSP00000512716.1:n.1314C>A
ENST00000696559.1:c.*156C>A ENSP00000512717.1:n.*156C>A
ENST00000696560.1:c.*156C>A ENSP00000512718.1:n.*156C>A
ENST00000696561.1:c.*156C>A ENSP00000512719.1:n.*156C>A
ENST00000696562.1:c.*156C>A ENSP00000512720.1:n.*156C>A
ENST00000412585.7:c.*156C>A MANE Select ENSP00000399168.2:n.*156C>A
ENST00000412585.6:c.*156C>A ENSP00000399168.2:n.*156C>A
ENST00000481849.5:n.480C>A
ENST00000497377.5:n.644C>A
NM_005514.6:c.*156C>A NP_005505.2:n.*156C>A
XM_011514556.1:c.*156C>A XP_011512858.1:n.*156C>A
XM_011514557.1:c.*156C>A XP_011512859.1:n.*156C>A
XR_926175.1:n.1684C>A
NM_005514.7:c.*156C>A NP_005505.2:n.*156C>A
NM_005514.8:c.*156C>A MANE Select NP_005505.2:n.*156C>A
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