Canonical Allele Identifier: CA2677953977

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354443-C-CCCCCCCCCCCCCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354443_31354444insCCCCCCCCCCCCCT , CM000668.2:g.31354443_31354444insCCCCCCCCCCCCCT	GRCh38
NC_000006.11:g.31322220_31322221insCCCCCCCCCCCCCT , CM000668.1:g.31322220_31322221insCCCCCCCCCCCCCT	GRCh37
NC_000006.10:g.31430199_31430200insCCCCCCCCCCCCCT	NCBI36
NG_023187.1:g.7769_7770insAGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+35_3140+36insAGGGGGGGGGGGGG
ENST00000481849.6:n.3100+35_3100+36insAGGGGGGGGGGGGG
ENST00000497377.6:n.3007+35_3007+36insAGGGGGGGGGGGGG
ENST00000696558.1:c.1162+35_1162+36insAGGGGGGGGGGGGG	ENSP00000512716.1:n.1162+35_1162+36insAGGGGGGGGGGGGG
ENST00000696559.1:c.*4+35_*4+36insAGGGGGGGGGGGGG	ENSP00000512717.1:n.*4+35_*4+36insAGGGGGGGGGGGGG
ENST00000696560.1:c.*4+35_*4+36insAGGGGGGGGGGGGG	ENSP00000512718.1:n.*4+35_*4+36insAGGGGGGGGGGGGG
ENST00000696561.1:c.*4+35_*4+36insAGGGGGGGGGGGGG	ENSP00000512719.1:n.*4+35_*4+36insAGGGGGGGGGGGGG
ENST00000696562.1:c.*4+35_*4+36insAGGGGGGGGGGGGG	ENSP00000512720.1:n.*4+35_*4+36insAGGGGGGGGGGGGG
ENST00000412585.7:c.*4+35_*4+36insAGGGGGGGGGGGGG MANE Select	ENSP00000399168.2:n.*4+35_*4+36insAGGGGGGGGGGGGG
ENST00000412585.6:c.*4+35_*4+36insAGGGGGGGGGGGGG	ENSP00000399168.2:n.*4+35_*4+36insAGGGGGGGGGGGGG
ENST00000481849.5:n.328+35_328+36insAGGGGGGGGGGGGG
ENST00000497377.5:n.492+35_492+36insAGGGGGGGGGGGGG
NM_005514.6:c.*4+35_*4+36insAGGGGGGGGGGGGG	NP_005505.2:n.*4+35_*4+36insAGGGGGGGGGGGGG
XM_011514556.1:c.*4+35_*4+36insAGGGGGGGGGGGGG	XP_011512858.1:n.*4+35_*4+36insAGGGGGGGGGGGGG
XM_011514557.1:c.*4+35_*4+36insAGGGGGGGGGGGGG	XP_011512859.1:n.*4+35_*4+36insAGGGGGGGGGGGGG
XR_926175.1:n.1532+35_1532+36insAGGGGGGGGGGGGG
NM_005514.7:c.*4+35_*4+36insAGGGGGGGGGGGGG	NP_005505.2:n.*4+35_*4+36insAGGGGGGGGGGGGG
NM_005514.8:c.*4+35_*4+36insAGGGGGGGGGGGGG MANE Select	NP_005505.2:n.*4+35_*4+36insAGGGGGGGGGGGGG