Canonical Allele Identifier: CA115644
Gene: HSPB8 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 2618
dbSNP Id: rs104894351

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.119187078A>G , CM000674.2:g.119187078A>G GRCh38
NC_000012.11:g.119624883A>G , CM000674.1:g.119624883A>G GRCh37
NC_000012.10:g.118109266A>G NCBI36
NG_007953.2:g.13289A>G , LRG_249:g.13289A>G

Transcript Alleles

HGVS Amino-acid change
NM_014365.2:c.421A>G , LRG_249t1:c.421A>G NP_055180.1:p.Lys141Glu
ENST00000281938.6:c.421A>G ENSP00000281938.2:p.Lys141Glu
ENST00000541798.1:n.144A>G
ENST00000542496.1:n.279A>G