Canonical Allele Identifier: CA2066828420

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119186990T= , CM000674.2:g.119186990T=	GRCh38
NC_000012.11:g.119624795T= , CM000674.1:g.119624795T=	GRCh37
NC_000012.10:g.118109178T=	NCBI36
NG_007953.2:g.13201T= , LRG_249:g.13201T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.368-35T= MANE Select	ENSP00000281938.3:n.368-35T=
ENST00000674542.1:c.368-6709T=	ENSP00000502352.1:n.368-6709T=
ENST00000674715.1:n.541-35T=
ENST00000675900.1:n.21+4954T=
ENST00000676071.1:n.101-35T=
ENST00000676244.1:n.74-35T=
ENST00000281938.6:c.368-35T=	ENSP00000281938.2:n.368-35T=
ENST00000541798.1:c.91-35T=
ENST00000542496.1:n.191T=
NM_014365.2:c.368-35T= , LRG_249t1:c.368-35T=	NP_055180.1:n.368-35T=
NM_014365.3:c.368-35T= MANE Select	NP_055180.1:n.368-35T=