Canonical Allele Identifier: CA136836306

Gene: HLA-B

Linked Data

• dbSNP Id: rs41559314
• gnomAD v4: 6-31356690-G-C
• MyVariant Identifiers: chr6:g.31324467G>C (hg19) ; chr6:g.31356690G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356690G>C , CM000668.2:g.31356690G>C	GRCh38
NC_000006.11:g.31324467G>C , CM000668.1:g.31324467G>C	GRCh37
NC_000006.10:g.31432446G>C	NCBI36
NG_023187.1:g.5523C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1814C>G
ENST00000481849.6:n.1814C>G
ENST00000497377.6:n.1814C>G
ENST00000640094.2:c.341C>G	ENSP00000491275.2:p.Ala114Gly
ENST00000696558.1:c.341C>G	ENSP00000512716.1:p.Ala114Gly
ENST00000696559.1:c.341C>G	ENSP00000512717.1:p.Ala114Gly
ENST00000696560.1:c.341C>G	ENSP00000512718.1:p.Ala114Gly
ENST00000696561.1:c.341C>G	ENSP00000512719.1:p.Ala114Gly
ENST00000696562.1:c.341C>G	ENSP00000512720.1:p.Ala114Gly
ENST00000412585.7:c.341C>G MANE Select	ENSP00000399168.2:p.Ala114Gly
ENST00000412585.6:c.341C>G	ENSP00000399168.2:p.Ala114Gly
ENST00000434333.1:c.374C>G	ENSP00000405931.1:p.Ala125Gly
ENST00000474381.1:n.216C>G
ENST00000498007.1:n.362C>G
ENST00000603274.1:n.44G>C
NM_005514.6:c.341C>G	NP_005505.2:p.Ala114Gly
XM_011514556.1:c.374C>G	XP_011512858.1:p.Ala125Gly
XM_011514557.1:c.341C>G	XP_011512859.1:p.Ala114Gly
XR_926175.1:n.351C>G
NM_005514.7:c.341C>G	NP_005505.2:p.Ala114Gly
NM_005514.8:c.341C>G MANE Select	NP_005505.2:p.Ala114Gly