Canonical Allele Identifier: CA419896026
Gene: CASQ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.116310938G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768317G>T , CM000663.2:g.115768317G>T GRCh38
NC_000001.10:g.116310938G>T , CM000663.1:g.116310938G>T GRCh37
NC_000001.9:g.116112461G>T NCBI36
NG_008802.1:g.5489C>A , LRG_404:g.5489C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-52C>A ENSP00000518226.1:n.-52C>A
ENST00000261448.6:c.225C>A MANE Select ENSP00000261448.5:p.Ile75=
ENST00000261448.5:c.225C>A ENSP00000261448.5:p.Ile75=
NM_001232.3:c.225C>A , LRG_404t1:c.225C>A NP_001223.2:p.Ile75=
NM_001232.4:c.225C>A MANE Select NP_001223.2:p.Ile75=