Canonical Allele Identifier: CA2677954823

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355076-A-ACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355077_31355078insAGC , CM000668.2:g.31355077_31355078insAGC	GRCh38
NC_000006.11:g.31322854_31322855insAGC , CM000668.1:g.31322854_31322855insAGC	GRCh37
NC_000006.10:g.31430833_31430834insAGC	NCBI36
NG_023187.1:g.7136_7137insCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+30_3059+31insCTG
ENST00000481849.6:n.2608_2609insCTG
ENST00000497377.6:n.2515_2516insCTG
ENST00000640094.2:c.895+240_895+241insCTG	ENSP00000491275.2:n.895+240_895+241insCTG
ENST00000696558.1:c.1081+30_1081+31insCTG	ENSP00000512716.1:n.1081+30_1081+31insCTG
ENST00000696559.1:c.1012+30_1012+31insCTG	ENSP00000512717.1:n.1012+30_1012+31insCTG
ENST00000696560.1:c.1012+30_1012+31insCTG	ENSP00000512718.1:n.1012+30_1012+31insCTG
ENST00000696561.1:c.1012+30_1012+31insCTG	ENSP00000512719.1:n.1012+30_1012+31insCTG
ENST00000696562.1:c.1012+30_1012+31insCTG	ENSP00000512720.1:n.1012+30_1012+31insCTG
ENST00000412585.7:c.1012+30_1012+31insCTG MANE Select	ENSP00000399168.2:n.1012+30_1012+31insCTG
ENST00000640094.1:c.88+240_88+241insCTG	ENSP00000491275.1:n.88+240_88+241insCTG
ENST00000412585.6:c.1012+30_1012+31insCTG	ENSP00000399168.2:n.1012+30_1012+31insCTG
NM_005514.6:c.1012+30_1012+31insCTG	NP_005505.2:n.1012+30_1012+31insCTG
XM_011514556.1:c.1045+30_1045+31insCTG	XP_011512858.1:n.1045+30_1045+31insCTG
XM_011514557.1:c.895+240_895+241insCTG	XP_011512859.1:n.895+240_895+241insCTG
XR_926175.1:n.1451+30_1451+31insCTG
NM_005514.7:c.1012+30_1012+31insCTG	NP_005505.2:n.1012+30_1012+31insCTG
NM_005514.8:c.1012+30_1012+31insCTG MANE Select	NP_005505.2:n.1012+30_1012+31insCTG