Canonical Allele Identifier: CA2621253711

Gene: HSPB8

Linked Data

• gnomAD v4: 12-119187011-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187011T>C , CM000674.2:g.119187011T>C	GRCh38
NC_000012.11:g.119624816T>C , CM000674.1:g.119624816T>C	GRCh37
NC_000012.10:g.118109199T>C	NCBI36
NG_007953.2:g.13222T>C , LRG_249:g.13222T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.368-14T>C MANE Select	ENSP00000281938.3:n.368-14T>C
ENST00000674542.1:c.368-6688T>C	ENSP00000502352.1:n.368-6688T>C
ENST00000674715.1:n.541-14T>C
ENST00000675900.1:n.21+4975T>C
ENST00000676071.1:n.101-14T>C
ENST00000676244.1:n.74-14T>C
ENST00000281938.6:c.368-14T>C	ENSP00000281938.2:n.368-14T>C
ENST00000541798.1:c.91-14T>C
ENST00000542496.1:n.212T>C
NM_014365.2:c.368-14T>C , LRG_249t1:c.368-14T>C	NP_055180.1:n.368-14T>C
NM_014365.3:c.368-14T>C MANE Select	NP_055180.1:n.368-14T>C