Canonical Allele Identifier: CA2594586017

Gene: HLA-B

Linked Data

• dbSNP Id: rs2113734255
• gnomAD v3: 6-31354997-CCT-C
• gnomAD v4: 6-31354997-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354998_31354999del , CM000668.2:g.31354998_31354999del	GRCh38
NC_000006.11:g.31322775_31322776del , CM000668.1:g.31322775_31322776del	GRCh37
NC_000006.10:g.31430754_31430755del	NCBI36
NG_023187.1:g.7214_7215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+108_3059+109del
ENST00000481849.6:n.2686_2687del
ENST00000497377.6:n.2593_2594del
ENST00000640094.2:c.895+318_895+319del	ENSP00000491275.2:n.895+318_895+319del
ENST00000696558.1:c.1081+108_1081+109del	ENSP00000512716.1:n.1081+108_1081+109del
ENST00000696559.1:c.1012+108_1012+109del	ENSP00000512717.1:n.1012+108_1012+109del
ENST00000696560.1:c.1012+108_1012+109del	ENSP00000512718.1:n.1012+108_1012+109del
ENST00000696561.1:c.1012+108_1012+109del	ENSP00000512719.1:n.1012+108_1012+109del
ENST00000696562.1:c.1012+108_1012+109del	ENSP00000512720.1:n.1012+108_1012+109del
ENST00000412585.7:c.1012+108_1012+109del MANE Select	ENSP00000399168.2:n.1012+108_1012+109del
ENST00000640094.1:c.88+318_88+319del	ENSP00000491275.1:n.88+318_88+319del
ENST00000412585.6:c.1012+108_1012+109del	ENSP00000399168.2:n.1012+108_1012+109del
ENST00000497377.5:n.78_79del
NM_005514.6:c.1012+108_1012+109del	NP_005505.2:n.1012+108_1012+109del
XM_011514556.1:c.1045+108_1045+109del	XP_011512858.1:n.1045+108_1045+109del
XM_011514557.1:c.895+318_895+319del	XP_011512859.1:n.895+318_895+319del
XR_926175.1:n.1451+108_1451+109del
NM_005514.7:c.1012+108_1012+109del	NP_005505.2:n.1012+108_1012+109del
NM_005514.8:c.1012+108_1012+109del MANE Select	NP_005505.2:n.1012+108_1012+109del