Canonical Allele Identifier: CA341767035
Gene: CASQ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.116310963T>C (hg19) chr1:g.115768342T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768342T>C , CM000663.2:g.115768342T>C GRCh38
NC_000001.10:g.116310963T>C , CM000663.1:g.116310963T>C GRCh37
NC_000001.9:g.116112486T>C NCBI36
NG_008802.1:g.5464A>G , LRG_404:g.5464A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-77A>G ENSP00000518226.1:n.-77A>G
ENST00000261448.6:c.200A>G MANE Select ENSP00000261448.5:p.Gln67Arg
ENST00000261448.5:c.200A>G ENSP00000261448.5:p.Gln67Arg
NM_001232.3:c.200A>G , LRG_404t1:c.200A>G NP_001223.2:p.Gln67Arg
NM_001232.4:c.200A>G MANE Select NP_001223.2:p.Gln67Arg
Search 100 bp 5'
Search 100 bp 3'