Canonical Allele Identifier: CA363891865

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356369-C-G
• MyVariant Identifiers: chr6:g.31324146C>G (hg19) ; chr6:g.31356369C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356369C>G , CM000668.2:g.31356369C>G	GRCh38
NC_000006.11:g.31324146C>G , CM000668.1:g.31324146C>G	GRCh37
NC_000006.10:g.31432125C>G	NCBI36
NG_023187.1:g.5844G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1890G>C
ENST00000481849.6:n.1890G>C
ENST00000497377.6:n.1890G>C
ENST00000640094.2:c.417G>C	ENSP00000491275.2:p.Gln139His
ENST00000696558.1:c.417G>C	ENSP00000512716.1:p.Gln139His
ENST00000696559.1:c.417G>C	ENSP00000512717.1:p.Gln139His
ENST00000696560.1:c.417G>C	ENSP00000512718.1:p.Gln139His
ENST00000696561.1:c.417G>C	ENSP00000512719.1:p.Gln139His
ENST00000696562.1:c.417G>C	ENSP00000512720.1:p.Gln139His
ENST00000412585.7:c.417G>C MANE Select	ENSP00000399168.2:p.Gln139His
ENST00000412585.6:c.417G>C	ENSP00000399168.2:p.Gln139His
ENST00000434333.1:c.450G>C	ENSP00000405931.1:p.Gln150His
ENST00000474381.1:n.292G>C
ENST00000498007.1:n.683G>C
NM_005514.6:c.417G>C	NP_005505.2:p.Gln139His
XM_011514556.1:c.450G>C	XP_011512858.1:p.Gln150His
XM_011514557.1:c.417G>C	XP_011512859.1:p.Gln139His
XR_926175.1:n.427G>C
NM_005514.7:c.417G>C	NP_005505.2:p.Gln139His
NM_005514.8:c.417G>C MANE Select	NP_005505.2:p.Gln139His