Canonical Allele Identifier: CA449603908

Gene: HLA-B

Linked Data

• dbSNP Id: rs1767260931
• gnomAD v4: 6-31357623-T-C
• MyVariant Identifiers: chr6:g.31325400T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357623T>C , CM000668.2:g.31357623T>C	GRCh38
NC_000006.11:g.31325400T>C , CM000668.1:g.31325400T>C	GRCh37
NC_000006.10:g.31433379T>C	NCBI36
NG_023187.1:g.4590A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1329A>G
ENST00000481849.6:n.1329A>G
ENST00000497377.6:n.1329A>G
ENST00000696559.1:c.-145A>G	ENSP00000512717.1:n.-145A>G
ENST00000696560.1:c.-145A>G	ENSP00000512718.1:n.-145A>G
ENST00000696561.1:c.-145A>G	ENSP00000512719.1:n.-145A>G
ENST00000696562.1:c.-135-330A>G	ENSP00000512720.1:n.-135-330A>G
ENST00000603274.1:n.977T>C
XR_926692.1:n.155A>G