Canonical Allele Identifier: CA2621253718

Gene: HSPB8

Linked Data

• gnomAD v4: 12-119187117-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187117G>C , CM000674.2:g.119187117G>C	GRCh38
NC_000012.11:g.119624922G>C , CM000674.1:g.119624922G>C	GRCh37
NC_000012.10:g.118109305G>C	NCBI36
NG_007953.2:g.13328G>C , LRG_249:g.13328G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000281938.7:c.431+29G>C MANE Select	ENSP00000281938.3:n.431+29G>C
ENST00000674542.1:c.368-6582G>C	ENSP00000502352.1:n.368-6582G>C
ENST00000674715.1:n.604+29G>C
ENST00000674763.1:c.64+29G>C
ENST00000674852.1:c.64+29G>C
ENST00000675110.1:c.64+29G>C
ENST00000675211.1:c.64+29G>C
ENST00000675573.1:c.64+29G>C
ENST00000675900.1:n.21+5081G>C
ENST00000676071.1:n.164+29G>C
ENST00000676244.1:n.137+29G>C
ENST00000281938.6:c.431+29G>C	ENSP00000281938.2:n.431+29G>C
ENST00000541798.1:c.154+29G>C
ENST00000542496.1:n.289+29G>C
NM_014365.2:c.431+29G>C , LRG_249t1:c.431+29G>C	NP_055180.1:n.431+29G>C
NM_014365.3:c.431+29G>C MANE Select	NP_055180.1:n.431+29G>C