Canonical Allele Identifier: CA363315105

Gene: HLA-B

Linked Data

• dbSNP Id: rs1417633427
• gnomAD v2: 6-31324898-A-G
• gnomAD v4: 6-31357121-A-G
• COSMIC: COSM3861674
• MyVariant Identifiers: chr6:g.31324898A>G (hg19) ; chr6:g.31357121A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357121A>G , CM000668.2:g.31357121A>G	GRCh38
NC_000006.11:g.31324898A>G , CM000668.1:g.31324898A>G	GRCh37
NC_000006.10:g.31432877A>G	NCBI36
NG_023187.1:g.5092T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1511T>C
ENST00000481849.6:n.1511T>C
ENST00000497377.6:n.1511T>C
ENST00000640094.2:c.38T>C	ENSP00000491275.2:p.Leu13Pro
ENST00000696558.1:c.38T>C	ENSP00000512716.1:p.Leu13Pro
ENST00000696559.1:c.38T>C	ENSP00000512717.1:p.Leu13Pro
ENST00000696560.1:c.38T>C	ENSP00000512718.1:p.Leu13Pro
ENST00000696561.1:c.38T>C	ENSP00000512719.1:p.Leu13Pro
ENST00000696562.1:c.38T>C	ENSP00000512720.1:p.Leu13Pro
ENST00000412585.7:c.38T>C MANE Select	ENSP00000399168.2:p.Leu13Pro
ENST00000412585.6:c.38T>C	ENSP00000399168.2:p.Leu13Pro
ENST00000434333.1:c.-58T>C	ENSP00000405931.1:n.-58T>C
ENST00000498007.1:n.59T>C
ENST00000603274.1:n.475A>G
NM_005514.6:c.38T>C	NP_005505.2:p.Leu13Pro
XM_011514557.1:c.38T>C	XP_011512859.1:p.Leu13Pro
XR_926175.1:n.48T>C
NM_005514.7:c.38T>C	NP_005505.2:p.Leu13Pro
NM_005514.8:c.38T>C MANE Select	NP_005505.2:p.Leu13Pro