Canonical Allele Identifier: CA2621253709

Gene: HSPB8

Linked Data

• gnomAD v4: 12-119187005-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187005C>T , CM000674.2:g.119187005C>T	GRCh38
NC_000012.11:g.119624810C>T , CM000674.1:g.119624810C>T	GRCh37
NC_000012.10:g.118109193C>T	NCBI36
NG_007953.2:g.13216C>T , LRG_249:g.13216C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.368-20C>T MANE Select	ENSP00000281938.3:n.368-20C>T
ENST00000674542.1:c.368-6694C>T	ENSP00000502352.1:n.368-6694C>T
ENST00000674715.1:n.541-20C>T
ENST00000675900.1:n.21+4969C>T
ENST00000676071.1:n.101-20C>T
ENST00000676244.1:n.74-20C>T
ENST00000281938.6:c.368-20C>T	ENSP00000281938.2:n.368-20C>T
ENST00000541798.1:c.91-20C>T
ENST00000542496.1:n.206C>T
NM_014365.2:c.368-20C>T , LRG_249t1:c.368-20C>T	NP_055180.1:n.368-20C>T
NM_014365.3:c.368-20C>T MANE Select	NP_055180.1:n.368-20C>T