Canonical Allele Identifier: CA6819623

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119193801A>G , CM000674.2:g.119193801A>G	GRCh38
NC_000012.11:g.119631606A>G , CM000674.1:g.119631606A>G	GRCh37
NC_000012.10:g.118115989A>G	NCBI36
NG_007953.2:g.20012A>G , LRG_249:g.20012A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.534A>G MANE Select	ENSP00000281938.3:p.Gly178=
ENST00000674542.1:c.*77A>G	ENSP00000502352.1:n.*77A>G
ENST00000674715.1:n.707A>G
ENST00000674763.1:c.239A>G
ENST00000674852.1:c.64+6713A>G
ENST00000675110.1:c.280A>G
ENST00000675211.1:c.297A>G
ENST00000675573.1:c.64+6713A>G
ENST00000675900.1:n.111A>G
ENST00000676071.1:n.267A>G
ENST00000676244.1:n.240A>G
ENST00000281938.6:c.534A>G	ENSP00000281938.2:p.Gly178=
ENST00000541798.1:c.154+6713A>G
ENST00000542496.1:n.392A>G
NM_014365.2:c.534A>G , LRG_249t1:c.534A>G	NP_055180.1:p.Gly178=
NM_014365.3:c.534A>G MANE Select	NP_055180.1:p.Gly178=