Canonical Allele Identifier: CA2677957870

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357071-C-CTAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357071_31357072insTAA , CM000668.2:g.31357071_31357072insTAA	GRCh38
NC_000006.11:g.31324848_31324849insTAA , CM000668.1:g.31324848_31324849insTAA	GRCh37
NC_000006.10:g.31432827_31432828insTAA	NCBI36
NG_023187.1:g.5141_5142insTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1546+14_1546+15insTTA
ENST00000481849.6:n.1546+14_1546+15insTTA
ENST00000497377.6:n.1546+14_1546+15insTTA
ENST00000640094.2:c.73+14_73+15insTTA	ENSP00000491275.2:n.73+14_73+15insTTA
ENST00000696558.1:c.73+14_73+15insTTA	ENSP00000512716.1:n.73+14_73+15insTTA
ENST00000696559.1:c.73+14_73+15insTTA	ENSP00000512717.1:n.73+14_73+15insTTA
ENST00000696560.1:c.73+14_73+15insTTA	ENSP00000512718.1:n.73+14_73+15insTTA
ENST00000696561.1:c.73+14_73+15insTTA	ENSP00000512719.1:n.73+14_73+15insTTA
ENST00000696562.1:c.73+14_73+15insTTA	ENSP00000512720.1:n.73+14_73+15insTTA
ENST00000412585.7:c.73+14_73+15insTTA MANE Select	ENSP00000399168.2:n.73+14_73+15insTTA
ENST00000412585.6:c.73+14_73+15insTTA	ENSP00000399168.2:n.73+14_73+15insTTA
ENST00000434333.1:c.-9_-8insTTA	ENSP00000405931.1:n.-9_-8insTTA
ENST00000498007.1:n.94+14_94+15insTTA
ENST00000603274.1:n.425_426insTAA
NM_005514.6:c.73+14_73+15insTTA	NP_005505.2:n.73+14_73+15insTTA
XM_011514556.1:c.-9_-8insTTA	XP_011512858.1:n.-9_-8insTTA
XM_011514557.1:c.73+14_73+15insTTA	XP_011512859.1:n.73+14_73+15insTTA
XR_926175.1:n.83+14_83+15insTTA
NM_005514.7:c.73+14_73+15insTTA	NP_005505.2:n.73+14_73+15insTTA
NM_005514.8:c.73+14_73+15insTTA MANE Select	NP_005505.2:n.73+14_73+15insTTA