Canonical Allele Identifier: CA449602260

Gene: HLA-B

Linked Data

• dbSNP Id: rs9266225
• gnomAD v3: 6-31357416-T-A
• gnomAD v4: 6-31357416-T-A
• MyVariant Identifiers: chr6:g.31325193T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357416T>A , CM000668.2:g.31357416T>A	GRCh38
NC_000006.11:g.31325193T>A , CM000668.1:g.31325193T>A	GRCh37
NC_000006.10:g.31433172T>A	NCBI36
NG_023187.1:g.4797A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1339-123A>T
ENST00000481849.6:n.1339-123A>T
ENST00000497377.6:n.1339-123A>T
ENST00000696559.1:c.-135-123A>T	ENSP00000512717.1:n.-135-123A>T
ENST00000696560.1:c.-135-123A>T	ENSP00000512718.1:n.-135-123A>T
ENST00000696561.1:c.-135-123A>T	ENSP00000512719.1:n.-135-123A>T
ENST00000696562.1:c.-135-123A>T	ENSP00000512720.1:n.-135-123A>T
ENST00000603274.1:n.770T>A
XR_926692.1:n.165-123A>T