Canonical Allele Identifier: CA566340063

Gene: HLA-B

Linked Data

• dbSNP Id: rs1215930005
• gnomAD v2: 6-31321866-C-T
• gnomAD v3: 6-31354089-C-T
• gnomAD v4: 6-31354089-C-T
• MyVariant Identifiers: chr6:g.31321866C>T (hg19) ; chr6:g.31354089C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354089C>T , CM000668.2:g.31354089C>T	GRCh38
NC_000006.11:g.31321866C>T , CM000668.1:g.31321866C>T	GRCh37
NC_000006.10:g.31429845C>T	NCBI36
NG_023187.1:g.8124G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3348G>A
ENST00000481849.6:n.3308G>A
ENST00000497377.6:n.3215G>A
ENST00000696558.1:c.1370G>A	ENSP00000512716.1:n.1370G>A
ENST00000696559.1:c.*212G>A	ENSP00000512717.1:n.*212G>A
ENST00000696560.1:c.*212G>A	ENSP00000512718.1:n.*212G>A
ENST00000696561.1:c.*212G>A	ENSP00000512719.1:n.*212G>A
ENST00000696562.1:c.*212G>A	ENSP00000512720.1:n.*212G>A
ENST00000412585.7:c.*212G>A MANE Select	ENSP00000399168.2:n.*212G>A
ENST00000412585.6:c.*212G>A	ENSP00000399168.2:n.*212G>A
ENST00000481849.5:n.536G>A
ENST00000497377.5:n.700G>A
NM_005514.6:c.*212G>A	NP_005505.2:n.*212G>A
XM_011514556.1:c.*212G>A	XP_011512858.1:n.*212G>A
XM_011514557.1:c.*212G>A	XP_011512859.1:n.*212G>A
XR_926175.1:n.1740G>A
NM_005514.7:c.*212G>A	NP_005505.2:n.*212G>A
NM_005514.8:c.*212G>A MANE Select	NP_005505.2:n.*212G>A