Canonical Allele Identifier: CA420178436
Gene: CASQ2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.116311058T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768437T>G , CM000663.2:g.115768437T>G GRCh38
NC_000001.10:g.116311058T>G , CM000663.1:g.116311058T>G GRCh37
NC_000001.9:g.116112581T>G NCBI36
NG_008802.1:g.5369A>C , LRG_404:g.5369A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-172A>C ENSP00000518226.1:n.-172A>C
ENST00000261448.6:c.105A>C MANE Select ENSP00000261448.5:p.Val35=
ENST00000261448.5:c.105A>C ENSP00000261448.5:p.Val35=
NM_001232.3:c.105A>C , LRG_404t1:c.105A>C NP_001223.2:p.Val35=
NM_001232.4:c.105A>C MANE Select NP_001223.2:p.Val35=
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Search 100 bp 3'