Canonical Allele Identifier: CA2677956932

Gene: HLA-B

Linked Data

• dbSNP Id: rs2113745912
• gnomAD v4: 6-31356431-G-GCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356431_31356432insCCA , CM000668.2:g.31356431_31356432insCCA	GRCh38
NC_000006.11:g.31324208_31324209insCCA , CM000668.1:g.31324208_31324209insCCA	GRCh37
NC_000006.10:g.31432187_31432188insCCA	NCBI36
NG_023187.1:g.5781_5782insTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1827_1828insTGG
ENST00000481849.6:n.1827_1828insTGG
ENST00000497377.6:n.1827_1828insTGG
ENST00000640094.2:c.354_355insTGG	ENSP00000491275.2:p.Thr118_Leu119insTrp
ENST00000696558.1:c.354_355insTGG	ENSP00000512716.1:p.Thr118_Leu119insTrp
ENST00000696559.1:c.354_355insTGG	ENSP00000512717.1:p.Thr118_Leu119insTrp
ENST00000696560.1:c.354_355insTGG	ENSP00000512718.1:p.Thr118_Leu119insTrp
ENST00000696561.1:c.354_355insTGG	ENSP00000512719.1:p.Thr118_Leu119insTrp
ENST00000696562.1:c.354_355insTGG	ENSP00000512720.1:p.Thr118_Leu119insTrp
ENST00000412585.7:c.354_355insTGG MANE Select	ENSP00000399168.2:p.Thr118_Leu119insTrp
ENST00000412585.6:c.354_355insTGG	ENSP00000399168.2:p.Thr118_Leu119insTrp
ENST00000434333.1:c.387_388insTGG	ENSP00000405931.1:p.Thr129_Leu130insTrp
ENST00000474381.1:n.229_230insTGG
ENST00000498007.1:n.620_621insTGG
NM_005514.6:c.354_355insTGG	NP_005505.2:p.Thr118_Leu119insTrp
XM_011514556.1:c.387_388insTGG	XP_011512858.1:p.Thr129_Leu130insTrp
XM_011514557.1:c.354_355insTGG	XP_011512859.1:p.Thr118_Leu119insTrp
XR_926175.1:n.364_365insTGG
NM_005514.7:c.354_355insTGG	NP_005505.2:p.Thr118_Leu119insTrp
NM_005514.8:c.354_355insTGG MANE Select	NP_005505.2:p.Thr118_Leu119insTrp