Canonical Allele Identifier: CA2677955313

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355470-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355471_31355472insCTG , CM000668.2:g.31355471_31355472insCTG	GRCh38
NC_000006.11:g.31323248_31323249insCTG , CM000668.1:g.31323248_31323249insCTG	GRCh37
NC_000006.10:g.31431227_31431228insCTG	NCBI36
NG_023187.1:g.6742_6743insAGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2788_2789insAGC
ENST00000481849.6:n.2214_2215insAGC
ENST00000497377.6:n.2214_2215insAGC
ENST00000640094.2:c.741_742insAGC	ENSP00000491275.2:p.Asp247_Gln248insSer
ENST00000696558.1:c.810_811insAGC	ENSP00000512716.1:n.810_811insAGC
ENST00000696559.1:c.741_742insAGC	ENSP00000512717.1:p.Asp247_Gln248insSer
ENST00000696560.1:c.741_742insAGC	ENSP00000512718.1:p.Asp247_Gln248insSer
ENST00000696561.1:c.741_742insAGC	ENSP00000512719.1:p.Asp247_Gln248insSer
ENST00000696562.1:c.741_742insAGC	ENSP00000512720.1:p.Asp247_Gln248insSer
ENST00000412585.7:c.741_742insAGC MANE Select	ENSP00000399168.2:p.Asp247_Gln248insSer
ENST00000412585.6:c.741_742insAGC	ENSP00000399168.2:p.Asp247_Gln248insSer
ENST00000463574.1:n.332_333insAGC
ENST00000498007.1:n.1007_1008insAGC
NM_005514.6:c.741_742insAGC	NP_005505.2:p.Asp247_Gln248insSer
XM_011514556.1:c.774_775insAGC	XP_011512858.1:p.Asp258_Gln259insSer
XM_011514557.1:c.741_742insAGC	XP_011512859.1:p.Asp247_Gln248insSer
XR_926175.1:n.1180_1181insAGC
NM_005514.7:c.741_742insAGC	NP_005505.2:p.Asp247_Gln248insSer
NM_005514.8:c.741_742insAGC MANE Select	NP_005505.2:p.Asp247_Gln248insSer