Canonical Allele Identifier: CA2621253708

Gene: HSPB8

Linked Data

• gnomAD v4: 12-119187000-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187000C>G , CM000674.2:g.119187000C>G	GRCh38
NC_000012.11:g.119624805C>G , CM000674.1:g.119624805C>G	GRCh37
NC_000012.10:g.118109188C>G	NCBI36
NG_007953.2:g.13211C>G , LRG_249:g.13211C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281938.7:c.368-25C>G MANE Select	ENSP00000281938.3:n.368-25C>G
ENST00000674542.1:c.368-6699C>G	ENSP00000502352.1:n.368-6699C>G
ENST00000674715.1:n.541-25C>G
ENST00000675900.1:n.21+4964C>G
ENST00000676071.1:n.101-25C>G
ENST00000676244.1:n.74-25C>G
ENST00000281938.6:c.368-25C>G	ENSP00000281938.2:n.368-25C>G
ENST00000541798.1:c.91-25C>G
ENST00000542496.1:n.201C>G
NM_014365.2:c.368-25C>G , LRG_249t1:c.368-25C>G	NP_055180.1:n.368-25C>G
NM_014365.3:c.368-25C>G MANE Select	NP_055180.1:n.368-25C>G