Canonical Allele Identifier: CA29605242
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs1034176201
MyVariant Identifiers: chr1:g.116243418A>T (hg19) chr1:g.115700797A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115700797A>T , CM000663.2:g.115700797A>T GRCh38
NC_000001.10:g.116243418A>T , CM000663.1:g.116243418A>T GRCh37
NC_000001.9:g.116044941A>T NCBI36
NG_008802.1:g.73009T>A , LRG_404:g.73009T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.*1016T>A ENSP00000518226.1:n.*1016T>A
ENST00000261448.6:c.*444T>A MANE Select ENSP00000261448.5:n.*444T>A
ENST00000261448.5:c.*444T>A ENSP00000261448.5:n.*444T>A
NM_001232.3:c.*444T>A , LRG_404t1:c.*444T>A NP_001223.2:n.*444T>A
NM_001232.4:c.*444T>A MANE Select NP_001223.2:n.*444T>A
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