Canonical Allele Identifier: CA363310609

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31323201C>A (hg19) ; chr6:g.31355424C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355424C>A , CM000668.2:g.31355424C>A	GRCh38
NC_000006.11:g.31323201C>A , CM000668.1:g.31323201C>A	GRCh37
NC_000006.10:g.31431180C>A	NCBI36
NG_023187.1:g.6789G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2835G>T
ENST00000481849.6:n.2261G>T
ENST00000497377.6:n.2261G>T
ENST00000640094.2:c.788G>T	ENSP00000491275.2:p.Arg263Ile
ENST00000696558.1:c.857G>T	ENSP00000512716.1:n.857G>T
ENST00000696559.1:c.788G>T	ENSP00000512717.1:p.Arg263Ile
ENST00000696560.1:c.788G>T	ENSP00000512718.1:p.Arg263Ile
ENST00000696561.1:c.788G>T	ENSP00000512719.1:p.Arg263Ile
ENST00000696562.1:c.788G>T	ENSP00000512720.1:p.Arg263Ile
ENST00000412585.7:c.788G>T MANE Select	ENSP00000399168.2:p.Arg263Ile
ENST00000412585.6:c.788G>T	ENSP00000399168.2:p.Arg263Ile
ENST00000463574.1:n.379G>T
ENST00000498007.1:n.1054G>T
NM_005514.6:c.788G>T	NP_005505.2:p.Arg263Ile
XM_011514556.1:c.821G>T	XP_011512858.1:p.Arg274Ile
XM_011514557.1:c.788G>T	XP_011512859.1:p.Arg263Ile
XR_926175.1:n.1227G>T
NM_005514.7:c.788G>T	NP_005505.2:p.Arg263Ile
NM_005514.8:c.788G>T MANE Select	NP_005505.2:p.Arg263Ile