Canonical Allele Identifier: CA2066828422

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119186993A= , CM000674.2:g.119186993A=	GRCh38
NC_000012.11:g.119624798A= , CM000674.1:g.119624798A=	GRCh37
NC_000012.10:g.118109181A=	NCBI36
NG_007953.2:g.13204A= , LRG_249:g.13204A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281938.7:c.368-32A= MANE Select	ENSP00000281938.3:n.368-32A=
ENST00000674542.1:c.368-6706A=	ENSP00000502352.1:n.368-6706A=
ENST00000674715.1:n.541-32A=
ENST00000675900.1:n.21+4957A=
ENST00000676071.1:n.101-32A=
ENST00000676244.1:n.74-32A=
ENST00000281938.6:c.368-32A=	ENSP00000281938.2:n.368-32A=
ENST00000541798.1:c.91-32A=
ENST00000542496.1:n.194A=
NM_014365.2:c.368-32A= , LRG_249t1:c.368-32A=	NP_055180.1:n.368-32A=
NM_014365.3:c.368-32A= MANE Select	NP_055180.1:n.368-32A=