Canonical Allele Identifier: CA136836131

Gene: HLA-B

Linked Data

• dbSNP Id: rs796284890

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356429_31356432delinsCCAA , CM000668.2:g.31356429_31356432delinsCCAA	GRCh38
NC_000006.11:g.31324206_31324209delinsCCAA , CM000668.1:g.31324206_31324209delinsCCAA	GRCh37
NC_000006.10:g.31432185_31432188delinsCCAA	NCBI36
NG_023187.1:g.5781_5784delinsTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1827_1830delinsTTGG
ENST00000481849.6:n.1827_1830delinsTTGG
ENST00000497377.6:n.1827_1830delinsTTGG
ENST00000640094.2:c.354_357delinsTTGG	ENSP00000491275.2:p.Leu119Trp
ENST00000696558.1:c.354_357delinsTTGG	ENSP00000512716.1:p.Leu119Trp
ENST00000696559.1:c.354_357delinsTTGG	ENSP00000512717.1:p.Leu119Trp
ENST00000696560.1:c.354_357delinsTTGG	ENSP00000512718.1:p.Leu119Trp
ENST00000696561.1:c.354_357delinsTTGG	ENSP00000512719.1:p.Leu119Trp
ENST00000696562.1:c.354_357delinsTTGG	ENSP00000512720.1:p.Leu119Trp
ENST00000412585.7:c.354_357delinsTTGG MANE Select	ENSP00000399168.2:p.Leu119Trp
ENST00000412585.6:c.354_357delinsTTGG	ENSP00000399168.2:p.Leu119Trp
ENST00000434333.1:c.387_390delinsTTGG	ENSP00000405931.1:p.Leu130Trp
ENST00000474381.1:n.229_232delinsTTGG
ENST00000498007.1:n.620_623delinsTTGG
NM_005514.6:c.354_357delinsTTGG	NP_005505.2:p.Leu119Trp
XM_011514556.1:c.387_390delinsTTGG	XP_011512858.1:p.Leu130Trp
XM_011514557.1:c.354_357delinsTTGG	XP_011512859.1:p.Leu119Trp
XR_926175.1:n.364_367delinsTTGG
NM_005514.7:c.354_357delinsTTGG	NP_005505.2:p.Leu119Trp
NM_005514.8:c.354_357delinsTTGG MANE Select	NP_005505.2:p.Leu119Trp