Canonical Allele Identifier: CA136832413

Gene: HLA-B

Linked Data

• dbSNP Id: rs879801545

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355133_31355134delinsT , CM000668.2:g.31355133_31355134delinsT	GRCh38
NC_000006.11:g.31322910_31322911delinsT , CM000668.1:g.31322910_31322911delinsT	GRCh37
NC_000006.10:g.31430889_31430890delinsT	NCBI36
NG_023187.1:g.7079_7080delinsA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3032_3033delinsA
ENST00000481849.6:n.2551_2552delinsA
ENST00000497377.6:n.2458_2459delinsA
ENST00000640094.2:c.895+183_895+184delinsA	ENSP00000491275.2:n.895+183_895+184delins...
ENST00000696558.1:c.1054_1055delinsA	ENSP00000512716.1:n.1054_1055delinsA
ENST00000696559.1:c.985_986delinsA	ENSP00000512717.1:p.Ala329MetfsTer2
ENST00000696560.1:c.985_986delinsA	ENSP00000512718.1:p.Ala329MetfsTer2
ENST00000696561.1:c.985_986delinsA	ENSP00000512719.1:p.Ala329MetfsTer2
ENST00000696562.1:c.985_986delinsA	ENSP00000512720.1:p.Ala329MetfsTer2
ENST00000412585.7:c.985_986delinsA MANE Select	ENSP00000399168.2:p.Ala329MetfsTer2
ENST00000640094.1:c.88+183_88+184delinsA	ENSP00000491275.1:n.88+183_88+184delinsA
ENST00000412585.6:c.985_986delinsA	ENSP00000399168.2:p.Ala329MetfsTer2
ENST00000463574.1:n.576_577delinsA
NM_005514.6:c.985_986delinsA	NP_005505.2:p.Ala329MetfsTer2
XM_011514556.1:c.1018_1019delinsA	XP_011512858.1:p.Ala340MetfsTer2
XM_011514557.1:c.895+183_895+184delinsA	XP_011512859.1:n.895+183_895+184delinsA
XR_926175.1:n.1424_1425delinsA
NM_005514.7:c.985_986delinsA	NP_005505.2:p.Ala329MetfsTer2
NM_005514.8:c.985_986delinsA MANE Select	NP_005505.2:p.Ala329MetfsTer2