Canonical Allele Identifier: CA525631225
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs1319928670
gnomAD v2: 1-116311201-G-A
gnomAD v4: 1-115768580-G-A
MyVariant Identifiers: chr1:g.116311201G>A (hg19) chr1:g.115768580G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768580G>A , CM000663.2:g.115768580G>A GRCh38
NC_000001.10:g.116311201G>A , CM000663.1:g.116311201G>A GRCh37
NC_000001.9:g.116112724G>A NCBI36
NG_008802.1:g.5226C>T , LRG_404:g.5226C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-223-92C>T ENSP00000518226.1:n.-223-92C>T
ENST00000261448.6:c.-39C>T MANE Select ENSP00000261448.5:n.-39C>T
ENST00000261448.5:c.-39C>T ENSP00000261448.5:n.-39C>T
NM_001232.3:c.-39C>T , LRG_404t1:c.-39C>T NP_001223.2:n.-39C>T
NM_001232.4:c.-39C>T MANE Select NP_001223.2:n.-39C>T
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