Canonical Allele Identifier: CA2677954743

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355038-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355040_31355041del , CM000668.2:g.31355040_31355041del	GRCh38
NC_000006.11:g.31322817_31322818del , CM000668.1:g.31322817_31322818del	GRCh37
NC_000006.10:g.31430796_31430797del	NCBI36
NG_023187.1:g.7173_7174del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+67_3059+68del
ENST00000481849.6:n.2645_2646del
ENST00000497377.6:n.2552_2553del
ENST00000640094.2:c.895+277_895+278del	ENSP00000491275.2:n.895+277_895+278del
ENST00000696558.1:c.1081+67_1081+68del	ENSP00000512716.1:n.1081+67_1081+68del
ENST00000696559.1:c.1012+67_1012+68del	ENSP00000512717.1:n.1012+67_1012+68del
ENST00000696560.1:c.1012+67_1012+68del	ENSP00000512718.1:n.1012+67_1012+68del
ENST00000696561.1:c.1012+67_1012+68del	ENSP00000512719.1:n.1012+67_1012+68del
ENST00000696562.1:c.1012+67_1012+68del	ENSP00000512720.1:n.1012+67_1012+68del
ENST00000412585.7:c.1012+67_1012+68del MANE Select	ENSP00000399168.2:n.1012+67_1012+68del
ENST00000640094.1:c.88+277_88+278del	ENSP00000491275.1:n.88+277_88+278del
ENST00000412585.6:c.1012+67_1012+68del	ENSP00000399168.2:n.1012+67_1012+68del
ENST00000497377.5:n.37_38del
NM_005514.6:c.1012+67_1012+68del	NP_005505.2:n.1012+67_1012+68del
XM_011514556.1:c.1045+67_1045+68del	XP_011512858.1:n.1045+67_1045+68del
XM_011514557.1:c.895+277_895+278del	XP_011512859.1:n.895+277_895+278del
XR_926175.1:n.1451+67_1451+68del
NM_005514.7:c.1012+67_1012+68del	NP_005505.2:n.1012+67_1012+68del
NM_005514.8:c.1012+67_1012+68del MANE Select	NP_005505.2:n.1012+67_1012+68del