Canonical Allele Identifier: CA3711167

Gene: HLA-B

Linked Data

• dbSNP Id: rs1554209903
• ExAC: 6:31322229 A / AG
• gnomAD v4: 6-31354452-A-AG
• MyVariant Identifiers: chr6:g.31322229_31322230insG (hg19) ; chr6:g.31354452_31354453insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354452_31354453insG , CM000668.2:g.31354452_31354453insG	GRCh38
NC_000006.11:g.31322229_31322230insG , CM000668.1:g.31322229_31322230insG	GRCh37
NC_000006.10:g.31430208_31430209insG	NCBI36
NG_023187.1:g.7760_7761insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+26_3140+27insC
ENST00000481849.6:n.3100+26_3100+27insC
ENST00000497377.6:n.3007+26_3007+27insC
ENST00000696558.1:c.1162+26_1162+27insC	ENSP00000512716.1:n.1162+26_1162+27insC
ENST00000696559.1:c.*4+26_*4+27insC	ENSP00000512717.1:n.*4+26_*4+27insC
ENST00000696560.1:c.*4+26_*4+27insC	ENSP00000512718.1:n.*4+26_*4+27insC
ENST00000696561.1:c.*4+26_*4+27insC	ENSP00000512719.1:n.*4+26_*4+27insC
ENST00000696562.1:c.*4+26_*4+27insC	ENSP00000512720.1:n.*4+26_*4+27insC
ENST00000412585.7:c.*4+26_*4+27insC MANE Select	ENSP00000399168.2:n.*4+26_*4+27insC
ENST00000412585.6:c.*4+26_*4+27insC	ENSP00000399168.2:n.*4+26_*4+27insC
ENST00000481849.5:n.328+26_328+27insC
ENST00000497377.5:n.492+26_492+27insC
NM_005514.6:c.*4+26_*4+27insC	NP_005505.2:n.*4+26_*4+27insC
XM_011514556.1:c.*4+26_*4+27insC	XP_011512858.1:n.*4+26_*4+27insC
XM_011514557.1:c.*4+26_*4+27insC	XP_011512859.1:n.*4+26_*4+27insC
XR_926175.1:n.1532+26_1532+27insC
NM_005514.7:c.*4+26_*4+27insC	NP_005505.2:n.*4+26_*4+27insC
NM_005514.8:c.*4+26_*4+27insC MANE Select	NP_005505.2:n.*4+26_*4+27insC