Canonical Allele Identifier: CA136832240

Gene: HLA-B

Linked Data

• dbSNP Id: rs386699131

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354927_31354929delinsGTG , CM000668.2:g.31354927_31354929delinsGTG	GRCh38
NC_000006.11:g.31322704_31322706delinsGTG , CM000668.1:g.31322704_31322706delinsGTG	GRCh37
NC_000006.10:g.31430683_31430685delinsGTG	NCBI36
NG_023187.1:g.7284_7286delinsCAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+178_3059+180delinsCAC
ENST00000481849.6:n.2756_2758delinsCAC
ENST00000497377.6:n.2663_2665delinsCAC
ENST00000640094.2:c.896-264_896-262delinsCAC	ENSP00000491275.2:n.896-264_896-262delinsCAC
ENST00000696558.1:c.1081+178_1081+180delinsCAC	ENSP00000512716.1:n.1081+178_1081+180delinsCAC
ENST00000696559.1:c.1012+178_1012+180delinsCAC	ENSP00000512717.1:n.1012+178_1012+180delinsCAC
ENST00000696560.1:c.1012+178_1012+180delinsCAC	ENSP00000512718.1:n.1012+178_1012+180delinsCAC
ENST00000696561.1:c.1012+178_1012+180delinsCAC	ENSP00000512719.1:n.1012+178_1012+180delinsCAC
ENST00000696562.1:c.1012+178_1012+180delinsCAC	ENSP00000512720.1:n.1012+178_1012+180delinsCAC
ENST00000412585.7:c.1012+178_1012+180delinsCAC MANE Select	ENSP00000399168.2:n.1012+178_1012+180delinsCAC
ENST00000640094.1:c.89-264_89-262delinsCAC	ENSP00000491275.1:n.89-264_89-262delinsCAC
ENST00000412585.6:c.1012+178_1012+180delinsCAC	ENSP00000399168.2:n.1012+178_1012+180delinsCAC
ENST00000497377.5:n.148_150delinsCAC
NM_005514.6:c.1012+178_1012+180delinsCAC	NP_005505.2:n.1012+178_1012+180delinsCAC
XM_011514556.1:c.1045+178_1045+180delinsCAC	XP_011512858.1:n.1045+178_1045+180delinsCAC
XM_011514557.1:c.896-264_896-262delinsCAC	XP_011512859.1:n.896-264_896-262delinsCAC
XR_926175.1:n.1451+178_1451+180delinsCAC
NM_005514.7:c.1012+178_1012+180delinsCAC	NP_005505.2:n.1012+178_1012+180delinsCAC
NM_005514.8:c.1012+178_1012+180delinsCAC MANE Select	NP_005505.2:n.1012+178_1012+180delinsCAC