Canonical Allele Identifier: CA29639008
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs1046915155
gnomAD v3: 1-115731032-T-C
gnomAD v4: 1-115731032-T-C
MyVariant Identifiers: chr1:g.116273653T>C (hg19) chr1:g.115731032T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115731032T>C , CM000663.2:g.115731032T>C GRCh38
NC_000001.10:g.116273653T>C , CM000663.1:g.116273653T>C GRCh37
NC_000001.9:g.116075176T>C NCBI36
NG_008802.1:g.42774A>G , LRG_404:g.42774A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.425+1082A>G ENSP00000518226.1:n.425+1082A>G
ENST00000261448.6:c.606+1869A>G MANE Select ENSP00000261448.5:n.606+1869A>G
ENST00000261448.5:c.606+1869A>G ENSP00000261448.5:n.606+1869A>G
ENST00000488931.1:n.122+1082A>G
NM_001232.3:c.606+1869A>G , LRG_404t1:c.606+1869A>G NP_001223.2:n.606+1869A>G
NM_001232.4:c.606+1869A>G MANE Select NP_001223.2:n.606+1869A>G
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