Canonical Allele Identifier: CA449603804
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31357587-C-A
MyVariant Identifiers: chr6:g.31325364C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357587C>A , CM000668.2:g.31357587C>A GRCh38
NC_000006.11:g.31325364C>A , CM000668.1:g.31325364C>A GRCh37
NC_000006.10:g.31433343C>A NCBI36
NG_023187.1:g.4626G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+27G>T
ENST00000481849.6:n.1338+27G>T
ENST00000497377.6:n.1338+27G>T
ENST00000696559.1:c.-136+27G>T ENSP00000512717.1:n.-136+27G>T
ENST00000696560.1:c.-136+27G>T ENSP00000512718.1:n.-136+27G>T
ENST00000696561.1:c.-136+27G>T ENSP00000512719.1:n.-136+27G>T
ENST00000696562.1:c.-135-294G>T ENSP00000512720.1:n.-135-294G>T
ENST00000603274.1:n.941C>A
XR_926692.1:n.164+27G>T
Search 100 bp 5'
Search 100 bp 3'