Canonical Allele Identifier: CA419895489
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs1447782106

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738261G>T , CM000663.2:g.115738261G>T GRCh38
NC_000001.10:g.116280882G>T , CM000663.1:g.116280882G>T GRCh37
NC_000001.9:g.116082405G>T NCBI36
NG_008802.1:g.35545C>A , LRG_404:g.35545C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.219C>A ENSP00000518226.1:p.Ile73=
ENST00000261448.6:c.495C>A MANE Select ENSP00000261448.5:p.Ile165=
ENST00000261448.5:c.495C>A ENSP00000261448.5:p.Ile165=
NM_001232.3:c.495C>A , LRG_404t1:c.495C>A NP_001223.2:p.Ile165=
NM_001232.4:c.495C>A MANE Select NP_001223.2:p.Ile165=