Canonical Allele Identifier: CA2621253715

Gene: HSPB8

Linked Data

• gnomAD v4: 12-119187104-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187104T>A , CM000674.2:g.119187104T>A	GRCh38
NC_000012.11:g.119624909T>A , CM000674.1:g.119624909T>A	GRCh37
NC_000012.10:g.118109292T>A	NCBI36
NG_007953.2:g.13315T>A , LRG_249:g.13315T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.431+16T>A MANE Select	ENSP00000281938.3:n.431+16T>A
ENST00000674542.1:c.368-6595T>A	ENSP00000502352.1:n.368-6595T>A
ENST00000674715.1:n.604+16T>A
ENST00000674763.1:c.64+16T>A
ENST00000674852.1:c.64+16T>A
ENST00000675110.1:c.64+16T>A
ENST00000675211.1:c.64+16T>A
ENST00000675573.1:c.64+16T>A
ENST00000675900.1:n.21+5068T>A
ENST00000676071.1:n.164+16T>A
ENST00000676244.1:n.137+16T>A
ENST00000281938.6:c.431+16T>A	ENSP00000281938.2:n.431+16T>A
ENST00000541798.1:c.154+16T>A
ENST00000542496.1:n.289+16T>A
NM_014365.2:c.431+16T>A , LRG_249t1:c.431+16T>A	NP_055180.1:n.431+16T>A
NM_014365.3:c.431+16T>A MANE Select	NP_055180.1:n.431+16T>A