Canonical Allele Identifier: CA2621253710

Gene: HSPB8

Linked Data

• gnomAD v4: 12-119187007-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187007C>T , CM000674.2:g.119187007C>T	GRCh38
NC_000012.11:g.119624812C>T , CM000674.1:g.119624812C>T	GRCh37
NC_000012.10:g.118109195C>T	NCBI36
NG_007953.2:g.13218C>T , LRG_249:g.13218C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.368-18C>T MANE Select	ENSP00000281938.3:n.368-18C>T
ENST00000674542.1:c.368-6692C>T	ENSP00000502352.1:n.368-6692C>T
ENST00000674715.1:n.541-18C>T
ENST00000675900.1:n.21+4971C>T
ENST00000676071.1:n.101-18C>T
ENST00000676244.1:n.74-18C>T
ENST00000281938.6:c.368-18C>T	ENSP00000281938.2:n.368-18C>T
ENST00000541798.1:c.91-18C>T
ENST00000542496.1:n.208C>T
NM_014365.2:c.368-18C>T , LRG_249t1:c.368-18C>T	NP_055180.1:n.368-18C>T
NM_014365.3:c.368-18C>T MANE Select	NP_055180.1:n.368-18C>T