Canonical Allele Identifier: CA341763858
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs1283548162

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738259T>C , CM000663.2:g.115738259T>C GRCh38
NC_000001.10:g.116280880T>C , CM000663.1:g.116280880T>C GRCh37
NC_000001.9:g.116082403T>C NCBI36
NG_008802.1:g.35547A>G , LRG_404:g.35547A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.221A>G ENSP00000518226.1:p.Lys74Arg
ENST00000261448.6:c.497A>G MANE Select ENSP00000261448.5:p.Lys166Arg
ENST00000261448.5:c.497A>G ENSP00000261448.5:p.Lys166Arg
NM_001232.3:c.497A>G , LRG_404t1:c.497A>G NP_001223.2:p.Lys166Arg
NM_001232.4:c.497A>G MANE Select NP_001223.2:p.Lys166Arg