Canonical Allele Identifier: CA2575313676

Gene: HSPB8

Linked Data

• gnomAD v4: 12-119187115-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187115A>C , CM000674.2:g.119187115A>C	GRCh38
NC_000012.11:g.119624920A>C , CM000674.1:g.119624920A>C	GRCh37
NC_000012.10:g.118109303A>C	NCBI36
NG_007953.2:g.13326A>C , LRG_249:g.13326A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.431+27A>C MANE Select	ENSP00000281938.3:n.431+27A>C
ENST00000674542.1:c.368-6584A>C	ENSP00000502352.1:n.368-6584A>C
ENST00000674715.1:n.604+27A>C
ENST00000674763.1:c.64+27A>C
ENST00000674852.1:c.64+27A>C
ENST00000675110.1:c.64+27A>C
ENST00000675211.1:c.64+27A>C
ENST00000675573.1:c.64+27A>C
ENST00000675900.1:n.21+5079A>C
ENST00000676071.1:n.164+27A>C
ENST00000676244.1:n.137+27A>C
ENST00000281938.6:c.431+27A>C	ENSP00000281938.2:n.431+27A>C
ENST00000541798.1:c.154+27A>C
ENST00000542496.1:n.289+27A>C
NM_014365.2:c.431+27A>C , LRG_249t1:c.431+27A>C	NP_055180.1:n.431+27A>C
NM_014365.3:c.431+27A>C MANE Select	NP_055180.1:n.431+27A>C