Canonical Allele Identifier: CA2770503720

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356240_31356241insTT , CM000668.2:g.31356240_31356241insTT	GRCh38
NC_000006.11:g.31324017_31324018insTT , CM000668.1:g.31324017_31324018insTT	GRCh37
NC_000006.10:g.31431996_31431997insTT	NCBI36
NG_023187.1:g.5972_5973insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2018_2019insAA
ENST00000481849.6:n.2018_2019insAA
ENST00000497377.6:n.2018_2019insAA
ENST00000640094.2:c.545_546insAA	ENSP00000491275.2:p.Tyr183ThrfsTer?
ENST00000696558.1:c.545_546insAA	ENSP00000512716.1:p.Tyr183ThrfsTer?
ENST00000696559.1:c.545_546insAA	ENSP00000512717.1:p.Tyr183ThrfsTer?
ENST00000696560.1:c.545_546insAA	ENSP00000512718.1:p.Tyr183ThrfsTer?
ENST00000696561.1:c.545_546insAA	ENSP00000512719.1:p.Tyr183ThrfsTer?
ENST00000696562.1:c.545_546insAA	ENSP00000512720.1:p.Tyr183ThrfsTer?
ENST00000412585.7:c.545_546insAA MANE Select	ENSP00000399168.2:p.Tyr183ThrfsTer?
ENST00000412585.6:c.545_546insAA	ENSP00000399168.2:p.Tyr183ThrfsTer?
ENST00000434333.1:c.578_579insAA	ENSP00000405931.1:p.Tyr194ThrfsTer?
ENST00000474381.1:n.420_421insAA
ENST00000498007.1:n.811_812insAA
NM_005514.6:c.545_546insAA	NP_005505.2:p.Tyr183ThrfsTer?
XM_011514556.1:c.578_579insAA	XP_011512858.1:p.Tyr194ThrfsTer?
XM_011514557.1:c.545_546insAA	XP_011512859.1:p.Tyr183ThrfsTer?
XR_926175.1:n.555_556insAA
NM_005514.7:c.545_546insAA	NP_005505.2:p.Tyr183ThrfsTer?
NM_005514.8:c.545_546insAA MANE Select	NP_005505.2:p.Tyr183ThrfsTer?