Canonical Allele Identifier: CA1023858
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs756935347

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115732902C>G , CM000663.2:g.115732902C>G GRCh38
NC_000001.10:g.116275523C>G , CM000663.1:g.116275523C>G GRCh37
NC_000001.9:g.116077046C>G NCBI36
NG_008802.1:g.40904G>C , LRG_404:g.40904G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.329G>C ENSP00000518226.1:p.Gly110Ala
ENST00000261448.6:c.605G>C MANE Select ENSP00000261448.5:p.Gly202Ala
ENST00000261448.5:c.605G>C ENSP00000261448.5:p.Gly202Ala
ENST00000488931.1:n.26G>C
NM_001232.3:c.605G>C , LRG_404t1:c.605G>C NP_001223.2:p.Gly202Ala
NM_001232.4:c.605G>C MANE Select NP_001223.2:p.Gly202Ala