Canonical Allele Identifier: CA363892519

Gene: HLA-B

Linked Data

• dbSNP Id: rs41556614
• gnomAD v2: 6-31324561-A-C
• gnomAD v3: 6-31356784-A-C
• gnomAD v4: 6-31356784-A-C
• MyVariant Identifiers: chr6:g.31324561A>C (hg19) ; chr6:g.31356784A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356784A>C , CM000668.2:g.31356784A>C	GRCh38
NC_000006.11:g.31324561A>C , CM000668.1:g.31324561A>C	GRCh37
NC_000006.10:g.31432540A>C	NCBI36
NG_023187.1:g.5429T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1720T>G
ENST00000481849.6:n.1720T>G
ENST00000497377.6:n.1720T>G
ENST00000640094.2:c.247T>G	ENSP00000491275.2:p.Tyr83Asp
ENST00000696558.1:c.247T>G	ENSP00000512716.1:p.Tyr83Asp
ENST00000696559.1:c.247T>G	ENSP00000512717.1:p.Tyr83Asp
ENST00000696560.1:c.247T>G	ENSP00000512718.1:p.Tyr83Asp
ENST00000696561.1:c.247T>G	ENSP00000512719.1:p.Tyr83Asp
ENST00000696562.1:c.247T>G	ENSP00000512720.1:p.Tyr83Asp
ENST00000412585.7:c.247T>G MANE Select	ENSP00000399168.2:p.Tyr83Asp
ENST00000412585.6:c.247T>G	ENSP00000399168.2:p.Tyr83Asp
ENST00000434333.1:c.280T>G	ENSP00000405931.1:p.Tyr94Asp
ENST00000474381.1:n.122T>G
ENST00000498007.1:n.268T>G
ENST00000603274.1:n.138A>C
NM_005514.6:c.247T>G	NP_005505.2:p.Tyr83Asp
XM_011514556.1:c.280T>G	XP_011512858.1:p.Tyr94Asp
XM_011514557.1:c.247T>G	XP_011512859.1:p.Tyr83Asp
XR_926175.1:n.257T>G
NM_005514.7:c.247T>G	NP_005505.2:p.Tyr83Asp
NM_005514.8:c.247T>G MANE Select	NP_005505.2:p.Tyr83Asp