Canonical Allele Identifier: CA2066828432

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187023A= , CM000674.2:g.119187023A=	GRCh38
NC_000012.11:g.119624828A= , CM000674.1:g.119624828A=	GRCh37
NC_000012.10:g.118109211A=	NCBI36
NG_007953.2:g.13234A= , LRG_249:g.13234A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.368-2A= MANE Select	ENSP00000281938.3:n.368-2A=
ENST00000674542.1:c.368-6676A=	ENSP00000502352.1:n.368-6676A=
ENST00000674715.1:n.541-2A=
ENST00000675900.1:n.21+4987A=
ENST00000676071.1:n.101-2A=
ENST00000676244.1:n.74-2A=
ENST00000281938.6:c.368-2A=	ENSP00000281938.2:n.368-2A=
ENST00000541798.1:c.91-2A=
ENST00000542496.1:n.224A=
NM_014365.2:c.368-2A= , LRG_249t1:c.368-2A=	NP_055180.1:n.368-2A=
NM_014365.3:c.368-2A= MANE Select	NP_055180.1:n.368-2A=