Canonical Allele Identifier: CA244339995

Gene: HSPB8

Linked Data

• dbSNP Id: rs112471271
• MyVariant Identifiers: chr12:g.119624895T>C (hg19) ; chr12:g.119187090T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187090T>C , CM000674.2:g.119187090T>C	GRCh38
NC_000012.11:g.119624895T>C , CM000674.1:g.119624895T>C	GRCh37
NC_000012.10:g.118109278T>C	NCBI36
NG_007953.2:g.13301T>C , LRG_249:g.13301T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000281938.7:c.431+2T>C MANE Select	ENSP00000281938.3:n.431+2T>C
ENST00000674542.1:c.368-6609T>C	ENSP00000502352.1:n.368-6609T>C
ENST00000674715.1:n.604+2T>C
ENST00000674763.1:c.64+2T>C
ENST00000674852.1:c.64+2T>C
ENST00000675110.1:c.64+2T>C
ENST00000675211.1:c.64+2T>C
ENST00000675573.1:c.64+2T>C
ENST00000675900.1:n.21+5054T>C
ENST00000676071.1:n.164+2T>C
ENST00000676244.1:n.137+2T>C
ENST00000281938.6:c.431+2T>C	ENSP00000281938.2:n.431+2T>C
ENST00000541798.1:c.154+2T>C
ENST00000542496.1:n.289+2T>C
NM_014365.2:c.431+2T>C , LRG_249t1:c.431+2T>C	NP_055180.1:n.431+2T>C
NM_014365.3:c.431+2T>C MANE Select	NP_055180.1:n.431+2T>C