Canonical Allele Identifier: CA136836383

Gene: HLA-B

Linked Data

• ClinVar Variation Id: 2656395
• ClinVar RCV Id: RCV003431746
• dbSNP Id: rs77604250
• gnomAD v4: 6-31356713-G-C
• MyVariant Identifiers: chr6:g.31324490G>C (hg19) ; chr6:g.31356713G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356713G>C , CM000668.2:g.31356713G>C	GRCh38
NC_000006.11:g.31324490G>C , CM000668.1:g.31324490G>C	GRCh37
NC_000006.10:g.31432469G>C	NCBI36
NG_023187.1:g.5500C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1791C>G
ENST00000481849.6:n.1791C>G
ENST00000497377.6:n.1791C>G
ENST00000640094.2:c.318C>G	ENSP00000491275.2:p.Arg106=
ENST00000696558.1:c.318C>G	ENSP00000512716.1:p.Arg106=
ENST00000696559.1:c.318C>G	ENSP00000512717.1:p.Arg106=
ENST00000696560.1:c.318C>G	ENSP00000512718.1:p.Arg106=
ENST00000696561.1:c.318C>G	ENSP00000512719.1:p.Arg106=
ENST00000696562.1:c.318C>G	ENSP00000512720.1:p.Arg106=
ENST00000412585.7:c.318C>G MANE Select	ENSP00000399168.2:p.Arg106=
ENST00000412585.6:c.318C>G	ENSP00000399168.2:p.Arg106=
ENST00000434333.1:c.351C>G	ENSP00000405931.1:p.Arg117=
ENST00000474381.1:n.193C>G
ENST00000498007.1:n.339C>G
ENST00000603274.1:n.67G>C
NM_005514.6:c.318C>G	NP_005505.2:p.Arg106=
XM_011514556.1:c.351C>G	XP_011512858.1:p.Arg117=
XM_011514557.1:c.318C>G	XP_011512859.1:p.Arg106=
XR_926175.1:n.328C>G
NM_005514.7:c.318C>G	NP_005505.2:p.Arg106=
NM_005514.8:c.318C>G MANE Select	NP_005505.2:p.Arg106=