Canonical Allele Identifier: CA419896019
Gene: CASQ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.116310929C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768308C>T , CM000663.2:g.115768308C>T GRCh38
NC_000001.10:g.116310929C>T , CM000663.1:g.116310929C>T GRCh37
NC_000001.9:g.116112452C>T NCBI36
NG_008802.1:g.5498G>A , LRG_404:g.5498G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-43G>A ENSP00000518226.1:n.-43G>A
ENST00000261448.6:c.234G>A MANE Select ENSP00000261448.5:p.Glu78=
ENST00000261448.5:c.234G>A ENSP00000261448.5:p.Glu78=
NM_001232.3:c.234G>A , LRG_404t1:c.234G>A NP_001223.2:p.Glu78=
NM_001232.4:c.234G>A MANE Select NP_001223.2:p.Glu78=