Canonical Allele Identifier: CA136832220

Gene: HLA-B

Linked Data

• dbSNP Id: rs878897947

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354926_31354927delinsT , CM000668.2:g.31354926_31354927delinsT	GRCh38
NC_000006.11:g.31322703_31322704delinsT , CM000668.1:g.31322703_31322704delinsT	GRCh37
NC_000006.10:g.31430682_31430683delinsT	NCBI36
NG_023187.1:g.7286_7287delinsA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+180_3059+181delinsA
ENST00000481849.6:n.2758_2759delinsA
ENST00000497377.6:n.2665_2666delinsA
ENST00000640094.2:c.896-262_896-261delinsA	ENSP00000491275.2:n.896-262_896-261delinsA
ENST00000696558.1:c.1081+180_1081+181delinsA	ENSP00000512716.1:n.1081+180_1081+181delinsA
ENST00000696559.1:c.1012+180_1012+181delinsA	ENSP00000512717.1:n.1012+180_1012+181delinsA
ENST00000696560.1:c.1012+180_1012+181delinsA	ENSP00000512718.1:n.1012+180_1012+181delinsA
ENST00000696561.1:c.1012+180_1012+181delinsA	ENSP00000512719.1:n.1012+180_1012+181delinsA
ENST00000696562.1:c.1012+180_1012+181delinsA	ENSP00000512720.1:n.1012+180_1012+181delinsA
ENST00000412585.7:c.1012+180_1012+181delinsA MANE Select	ENSP00000399168.2:n.1012+180_1012+181delinsA
ENST00000640094.1:c.89-262_89-261delinsA	ENSP00000491275.1:n.89-262_89-261delinsA
ENST00000412585.6:c.1012+180_1012+181delinsA	ENSP00000399168.2:n.1012+180_1012+181delinsA
ENST00000497377.5:n.150_151delinsA
NM_005514.6:c.1012+180_1012+181delinsA	NP_005505.2:n.1012+180_1012+181delinsA
XM_011514556.1:c.1045+180_1045+181delinsA	XP_011512858.1:n.1045+180_1045+181delinsA
XM_011514557.1:c.896-262_896-261delinsA	XP_011512859.1:n.896-262_896-261delinsA
XR_926175.1:n.1451+180_1451+181delinsA
NM_005514.7:c.1012+180_1012+181delinsA	NP_005505.2:n.1012+180_1012+181delinsA
NM_005514.8:c.1012+180_1012+181delinsA MANE Select	NP_005505.2:n.1012+180_1012+181delinsA