Canonical Allele Identifier: CA2677954850

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355082-A-ACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355083_31355084insAGC , CM000668.2:g.31355083_31355084insAGC	GRCh38
NC_000006.11:g.31322860_31322861insAGC , CM000668.1:g.31322860_31322861insAGC	GRCh37
NC_000006.10:g.31430839_31430840insAGC	NCBI36
NG_023187.1:g.7130_7131insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+24_3059+25insCTG
ENST00000481849.6:n.2602_2603insCTG
ENST00000497377.6:n.2509_2510insCTG
ENST00000640094.2:c.895+234_895+235insCTG	ENSP00000491275.2:n.895+234_895+235insCTG
ENST00000696558.1:c.1081+24_1081+25insCTG	ENSP00000512716.1:n.1081+24_1081+25insCTG
ENST00000696559.1:c.1012+24_1012+25insCTG	ENSP00000512717.1:n.1012+24_1012+25insCTG
ENST00000696560.1:c.1012+24_1012+25insCTG	ENSP00000512718.1:n.1012+24_1012+25insCTG
ENST00000696561.1:c.1012+24_1012+25insCTG	ENSP00000512719.1:n.1012+24_1012+25insCTG
ENST00000696562.1:c.1012+24_1012+25insCTG	ENSP00000512720.1:n.1012+24_1012+25insCTG
ENST00000412585.7:c.1012+24_1012+25insCTG MANE Select	ENSP00000399168.2:n.1012+24_1012+25insCTG
ENST00000640094.1:c.88+234_88+235insCTG	ENSP00000491275.1:n.88+234_88+235insCTG
ENST00000412585.6:c.1012+24_1012+25insCTG	ENSP00000399168.2:n.1012+24_1012+25insCTG
NM_005514.6:c.1012+24_1012+25insCTG	NP_005505.2:n.1012+24_1012+25insCTG
XM_011514556.1:c.1045+24_1045+25insCTG	XP_011512858.1:n.1045+24_1045+25insCTG
XM_011514557.1:c.895+234_895+235insCTG	XP_011512859.1:n.895+234_895+235insCTG
XR_926175.1:n.1451+24_1451+25insCTG
NM_005514.7:c.1012+24_1012+25insCTG	NP_005505.2:n.1012+24_1012+25insCTG
NM_005514.8:c.1012+24_1012+25insCTG MANE Select	NP_005505.2:n.1012+24_1012+25insCTG