Canonical Allele Identifier: CA341767014
Gene: CASQ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.116310955A>C (hg19) chr1:g.115768334A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768334A>C , CM000663.2:g.115768334A>C GRCh38
NC_000001.10:g.116310955A>C , CM000663.1:g.116310955A>C GRCh37
NC_000001.9:g.116112478A>C NCBI36
NG_008802.1:g.5472T>G , LRG_404:g.5472T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-69T>G ENSP00000518226.1:n.-69T>G
ENST00000261448.6:c.208T>G MANE Select ENSP00000261448.5:p.Phe70Val
ENST00000261448.5:c.208T>G ENSP00000261448.5:p.Phe70Val
NM_001232.3:c.208T>G , LRG_404t1:c.208T>G NP_001223.2:p.Phe70Val
NM_001232.4:c.208T>G MANE Select NP_001223.2:p.Phe70Val
Search 100 bp 5'
Search 100 bp 3'