Canonical Allele Identifier: CA136836262

Gene: HLA-B

Linked Data

• dbSNP Id: rs281864609

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356595_31356598del , CM000668.2:g.31356595_31356598del	GRCh38
NC_000006.11:g.31324372_31324375del , CM000668.1:g.31324372_31324375del	GRCh37
NC_000006.10:g.31432351_31432354del	NCBI36
NG_023187.1:g.5618_5621del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1816+93_1816+96del
ENST00000481849.6:n.1816+93_1816+96del
ENST00000497377.6:n.1816+93_1816+96del
ENST00000640094.2:c.343+93_343+96del	ENSP00000491275.2:n.343+93_343+96del
ENST00000696558.1:c.343+93_343+96del	ENSP00000512716.1:n.343+93_343+96del
ENST00000696559.1:c.343+93_343+96del	ENSP00000512717.1:n.343+93_343+96del
ENST00000696560.1:c.343+93_343+96del	ENSP00000512718.1:n.343+93_343+96del
ENST00000696561.1:c.343+93_343+96del	ENSP00000512719.1:n.343+93_343+96del
ENST00000696562.1:c.343+93_343+96del	ENSP00000512720.1:n.343+93_343+96del
ENST00000412585.7:c.343+93_343+96del MANE Select	ENSP00000399168.2:n.343+93_343+96del
ENST00000412585.6:c.343+93_343+96del	ENSP00000399168.2:n.343+93_343+96del
ENST00000434333.1:c.376+93_376+96del	ENSP00000405931.1:n.376+93_376+96del
ENST00000474381.1:n.218+93_218+96del
ENST00000498007.1:n.457_460del
NM_005514.6:c.343+93_343+96del	NP_005505.2:n.343+93_343+96del
XM_011514556.1:c.376+93_376+96del	XP_011512858.1:n.376+93_376+96del
XM_011514557.1:c.343+93_343+96del	XP_011512859.1:n.343+93_343+96del
XR_926175.1:n.353+93_353+96del
NM_005514.7:c.343+93_343+96del	NP_005505.2:n.343+93_343+96del
NM_005514.8:c.343+93_343+96del MANE Select	NP_005505.2:n.343+93_343+96del