Canonical Allele Identifier: CA363310868

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31323241G>C (hg19) ; chr6:g.31355464G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355464G>C , CM000668.2:g.31355464G>C	GRCh38
NC_000006.11:g.31323241G>C , CM000668.1:g.31323241G>C	GRCh37
NC_000006.10:g.31431220G>C	NCBI36
NG_023187.1:g.6749C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2795C>G
ENST00000481849.6:n.2221C>G
ENST00000497377.6:n.2221C>G
ENST00000640094.2:c.748C>G	ENSP00000491275.2:p.Gln250Glu
ENST00000696558.1:c.817C>G	ENSP00000512716.1:n.817C>G
ENST00000696559.1:c.748C>G	ENSP00000512717.1:p.Gln250Glu
ENST00000696560.1:c.748C>G	ENSP00000512718.1:p.Gln250Glu
ENST00000696561.1:c.748C>G	ENSP00000512719.1:p.Gln250Glu
ENST00000696562.1:c.748C>G	ENSP00000512720.1:p.Gln250Glu
ENST00000412585.7:c.748C>G MANE Select	ENSP00000399168.2:p.Gln250Glu
ENST00000412585.6:c.748C>G	ENSP00000399168.2:p.Gln250Glu
ENST00000463574.1:n.339C>G
ENST00000498007.1:n.1014C>G
NM_005514.6:c.748C>G	NP_005505.2:p.Gln250Glu
XM_011514556.1:c.781C>G	XP_011512858.1:p.Gln261Glu
XM_011514557.1:c.748C>G	XP_011512859.1:p.Gln250Glu
XR_926175.1:n.1187C>G
NM_005514.7:c.748C>G	NP_005505.2:p.Gln250Glu
NM_005514.8:c.748C>G MANE Select	NP_005505.2:p.Gln250Glu