Canonical Allele Identifier: CA449790960

Gene: HLA-B

Linked Data

• dbSNP Id: rs1443678572
• gnomAD v2: 6-31324984-A-G
• gnomAD v4: 6-31357207-A-G
• MyVariant Identifiers: chr6:g.31324984A>G (hg19) ; chr6:g.31357207A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357207A>G , CM000668.2:g.31357207A>G	GRCh38
NC_000006.11:g.31324984A>G , CM000668.1:g.31324984A>G	GRCh37
NC_000006.10:g.31432963A>G	NCBI36
NG_023187.1:g.5006T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1425T>C
ENST00000481849.6:n.1425T>C
ENST00000497377.6:n.1425T>C
ENST00000696559.1:c.-49T>C	ENSP00000512717.1:n.-49T>C
ENST00000696560.1:c.-49T>C	ENSP00000512718.1:n.-49T>C
ENST00000696561.1:c.-49T>C	ENSP00000512719.1:n.-49T>C
ENST00000696562.1:c.-49T>C	ENSP00000512720.1:n.-49T>C
ENST00000603274.1:n.561A>G
NM_005514.6:c.-49T>C	NP_005505.2:n.-49T>C
NM_005514.7:c.-49T>C	NP_005505.2:n.-49T>C