Canonical Allele Identifier: CA363310333

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355375-C-A
• MyVariant Identifiers: chr6:g.31323152C>A (hg19) ; chr6:g.31355375C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355375C>A , CM000668.2:g.31355375C>A	GRCh38
NC_000006.11:g.31323152C>A , CM000668.1:g.31323152C>A	GRCh37
NC_000006.10:g.31431131C>A	NCBI36
NG_023187.1:g.6838G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2884G>T
ENST00000481849.6:n.2310G>T
ENST00000497377.6:n.2310G>T
ENST00000640094.2:c.837G>T	ENSP00000491275.2:p.Gln279His
ENST00000696558.1:c.906G>T	ENSP00000512716.1:n.906G>T
ENST00000696559.1:c.837G>T	ENSP00000512717.1:p.Gln279His
ENST00000696560.1:c.837G>T	ENSP00000512718.1:p.Gln279His
ENST00000696561.1:c.837G>T	ENSP00000512719.1:p.Gln279His
ENST00000696562.1:c.837G>T	ENSP00000512720.1:p.Gln279His
ENST00000412585.7:c.837G>T MANE Select	ENSP00000399168.2:p.Gln279His
ENST00000640094.1:c.30G>T	ENSP00000491275.1:p.Gln10His
ENST00000412585.6:c.837G>T	ENSP00000399168.2:p.Gln279His
ENST00000463574.1:n.428G>T
NM_005514.6:c.837G>T	NP_005505.2:p.Gln279His
XM_011514556.1:c.870G>T	XP_011512858.1:p.Gln290His
XM_011514557.1:c.837G>T	XP_011512859.1:p.Gln279His
XR_926175.1:n.1276G>T
NM_005514.7:c.837G>T	NP_005505.2:p.Gln279His
NM_005514.8:c.837G>T MANE Select	NP_005505.2:p.Gln279His