Canonical Allele Identifier: CA386529606
Gene: HSPB8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.119187085T>G , CM000674.2:g.119187085T>G GRCh38
NC_000012.11:g.119624890T>G , CM000674.1:g.119624890T>G GRCh37
NC_000012.10:g.118109273T>G NCBI36
NG_007953.2:g.13296T>G , LRG_249:g.13296T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000281938.7:c.428T>G MANE Select ENSP00000281938.3:p.Ile143Ser
ENST00000674542.1:c.368-6614T>G ENSP00000502352.1:n.368-6614T>G
ENST00000674715.1:n.601T>G
ENST00000674763.1:c.61T>G
ENST00000674852.1:c.61T>G
ENST00000675110.1:c.61T>G
ENST00000675211.1:c.61T>G
ENST00000675573.1:c.61T>G
ENST00000675900.1:n.21+5049T>G
ENST00000676071.1:n.161T>G
ENST00000676244.1:n.134T>G
ENST00000281938.6:c.428T>G ENSP00000281938.2:p.Ile143Ser
ENST00000541798.1:c.151T>G
ENST00000542496.1:n.286T>G
NM_014365.2:c.428T>G , LRG_249t1:c.428T>G NP_055180.1:p.Ile143Ser
NM_014365.3:c.428T>G MANE Select NP_055180.1:p.Ile143Ser