Canonical Allele Identifier: CA136836751

Gene: HLA-B

Linked Data

• dbSNP Id: rs949147688
• gnomAD v3: 6-31357186-G-C
• gnomAD v4: 6-31357186-G-C
• MyVariant Identifiers: chr6:g.31324963G>C (hg19) ; chr6:g.31357186G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357186G>C , CM000668.2:g.31357186G>C	GRCh38
NC_000006.11:g.31324963G>C , CM000668.1:g.31324963G>C	GRCh37
NC_000006.10:g.31432942G>C	NCBI36
NG_023187.1:g.5027C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1446C>G
ENST00000481849.6:n.1446C>G
ENST00000497377.6:n.1446C>G
ENST00000696559.1:c.-28C>G	ENSP00000512717.1:n.-28C>G
ENST00000696560.1:c.-28C>G	ENSP00000512718.1:n.-28C>G
ENST00000696561.1:c.-28C>G	ENSP00000512719.1:n.-28C>G
ENST00000696562.1:c.-28C>G	ENSP00000512720.1:n.-28C>G
ENST00000412585.6:c.-28C>G	ENSP00000399168.2:n.-28C>G
ENST00000434333.1:c.-123C>G	ENSP00000405931.1:n.-123C>G
ENST00000603274.1:n.540G>C
NM_005514.6:c.-28C>G	NP_005505.2:n.-28C>G
NM_005514.7:c.-28C>G	NP_005505.2:n.-28C>G