Canonical Allele Identifier: CA650785886

Gene: HLA-B

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354198_31354199insA , CM000668.2:g.31354198_31354199insA	GRCh38
NC_000006.11:g.31321975_31321976insA , CM000668.1:g.31321975_31321976insA	GRCh37
NC_000006.10:g.31429954_31429955insA	NCBI36
NG_023187.1:g.8014_8015insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3238_3239insT
ENST00000481849.6:n.3198_3199insT
ENST00000497377.6:n.3105_3106insT
ENST00000696558.1:c.1260_1261insT	ENSP00000512716.1:n.1260_1261insT
ENST00000696559.1:c.*102_*103insT	ENSP00000512717.1:n.*102_*103insT
ENST00000696560.1:c.*102_*103insT	ENSP00000512718.1:n.*102_*103insT
ENST00000696561.1:c.*102_*103insT	ENSP00000512719.1:n.*102_*103insT
ENST00000696562.1:c.*102_*103insT	ENSP00000512720.1:n.*102_*103insT
ENST00000412585.7:c.*102_*103insT MANE Select	ENSP00000399168.2:n.*102_*103insT
ENST00000412585.6:c.*102_*103insT	ENSP00000399168.2:n.*102_*103insT
ENST00000481849.5:n.426_427insT
ENST00000497377.5:n.590_591insT
NM_005514.6:c.*102_*103insT	NP_005505.2:n.*102_*103insT
XM_011514556.1:c.*102_*103insT	XP_011512858.1:n.*102_*103insT
XM_011514557.1:c.*102_*103insT	XP_011512859.1:n.*102_*103insT
XR_926175.1:n.1630_1631insT
NM_005514.7:c.*102_*103insT	NP_005505.2:n.*102_*103insT
NM_005514.8:c.*102_*103insT MANE Select	NP_005505.2:n.*102_*103insT