Canonical Allele Identifier: CA566340065

Gene: HLA-B

Linked Data

• dbSNP Id: rs1264126693
• gnomAD v2: 6-31321867-T-C
• gnomAD v3: 6-31354090-T-C
• gnomAD v4: 6-31354090-T-C
• MyVariant Identifiers: chr6:g.31321867T>C (hg19) ; chr6:g.31354090T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354090T>C , CM000668.2:g.31354090T>C	GRCh38
NC_000006.11:g.31321867T>C , CM000668.1:g.31321867T>C	GRCh37
NC_000006.10:g.31429846T>C	NCBI36
NG_023187.1:g.8123A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3347A>G
ENST00000481849.6:n.3307A>G
ENST00000497377.6:n.3214A>G
ENST00000696558.1:c.1369A>G	ENSP00000512716.1:n.1369A>G
ENST00000696559.1:c.*211A>G	ENSP00000512717.1:n.*211A>G
ENST00000696560.1:c.*211A>G	ENSP00000512718.1:n.*211A>G
ENST00000696561.1:c.*211A>G	ENSP00000512719.1:n.*211A>G
ENST00000696562.1:c.*211A>G	ENSP00000512720.1:n.*211A>G
ENST00000412585.7:c.*211A>G MANE Select	ENSP00000399168.2:n.*211A>G
ENST00000412585.6:c.*211A>G	ENSP00000399168.2:n.*211A>G
ENST00000481849.5:n.535A>G
ENST00000497377.5:n.699A>G
NM_005514.6:c.*211A>G	NP_005505.2:n.*211A>G
XM_011514556.1:c.*211A>G	XP_011512858.1:n.*211A>G
XM_011514557.1:c.*211A>G	XP_011512859.1:n.*211A>G
XR_926175.1:n.1739A>G
NM_005514.7:c.*211A>G	NP_005505.2:n.*211A>G
NM_005514.8:c.*211A>G MANE Select	NP_005505.2:n.*211A>G