Canonical Allele Identifier: CA449791024

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31357231-A-C
• gnomAD v4: 6-31357231-A-C
• MyVariant Identifiers: chr6:g.31325008A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357231A>C , CM000668.2:g.31357231A>C	GRCh38
NC_000006.11:g.31325008A>C , CM000668.1:g.31325008A>C	GRCh37
NC_000006.10:g.31432987A>C	NCBI36
NG_023187.1:g.4982T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1401T>G
ENST00000481849.6:n.1401T>G
ENST00000497377.6:n.1401T>G
ENST00000696559.1:c.-73T>G	ENSP00000512717.1:n.-73T>G
ENST00000696560.1:c.-73T>G	ENSP00000512718.1:n.-73T>G
ENST00000696561.1:c.-73T>G	ENSP00000512719.1:n.-73T>G
ENST00000696562.1:c.-73T>G	ENSP00000512720.1:n.-73T>G
ENST00000603274.1:n.585A>C
NM_005514.7:c.-73T>G	NP_005505.2:n.-73T>G