Canonical Allele Identifier: CA136836579

Gene: HLA-B

Linked Data

• dbSNP Id: rs199774565
• MyVariant Identifiers: chr6:g.31324593_31324594del (hg19) ; chr6:g.31356816_31356817del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356818_31356819del , CM000668.2:g.31356818_31356819del	GRCh38
NC_000006.11:g.31324595_31324596del , CM000668.1:g.31324595_31324596del	GRCh37
NC_000006.10:g.31432574_31432575del	NCBI36
NG_023187.1:g.5396_5397del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1687_1688del
ENST00000481849.6:n.1687_1688del
ENST00000497377.6:n.1687_1688del
ENST00000640094.2:c.214_215del	ENSP00000491275.2:p.Arg72GlyfsTer26
ENST00000696558.1:c.214_215del	ENSP00000512716.1:p.Arg72GlyfsTer26
ENST00000696559.1:c.214_215del	ENSP00000512717.1:p.Arg72GlyfsTer26
ENST00000696560.1:c.214_215del	ENSP00000512718.1:p.Arg72GlyfsTer26
ENST00000696561.1:c.214_215del	ENSP00000512719.1:p.Arg72GlyfsTer26
ENST00000696562.1:c.214_215del	ENSP00000512720.1:p.Arg72GlyfsTer26
ENST00000412585.7:c.214_215del MANE Select	ENSP00000399168.2:p.Arg72GlyfsTer26
ENST00000412585.6:c.214_215del	ENSP00000399168.2:p.Arg72GlyfsTer26
ENST00000434333.1:c.247_248del	ENSP00000405931.1:p.Arg83GlyfsTer26
ENST00000474381.1:n.89_90del
ENST00000498007.1:n.235_236del
ENST00000603274.1:n.172_173del
NM_005514.6:c.214_215del	NP_005505.2:p.Arg72GlyfsTer26
XM_011514556.1:c.247_248del	XP_011512858.1:p.Arg83GlyfsTer26
XM_011514557.1:c.214_215del	XP_011512859.1:p.Arg72GlyfsTer26
XR_926175.1:n.224_225del
NM_005514.7:c.214_215del	NP_005505.2:p.Arg72GlyfsTer26
NM_005514.8:c.214_215del MANE Select	NP_005505.2:p.Arg72GlyfsTer26