Canonical Allele Identifier: CA29603423
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs774051297
gnomAD v2: 1-116280678-C-T
gnomAD v3: 1-115738057-C-T
gnomAD v4: 1-115738057-C-T
MyVariant Identifiers: chr1:g.116280678C>T (hg19) chr1:g.115738057C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115738057C>T , CM000663.2:g.115738057C>T GRCh38
NC_000001.10:g.116280678C>T , CM000663.1:g.116280678C>T GRCh37
NC_000001.9:g.116082201C>T NCBI36
NG_008802.1:g.35749G>A , LRG_404:g.35749G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.256+167G>A ENSP00000518226.1:n.256+167G>A
ENST00000261448.6:c.532+167G>A MANE Select ENSP00000261448.5:n.532+167G>A
ENST00000261448.5:c.532+167G>A ENSP00000261448.5:n.532+167G>A
NM_001232.3:c.532+167G>A , LRG_404t1:c.532+167G>A NP_001223.2:n.532+167G>A
NM_001232.4:c.532+167G>A MANE Select NP_001223.2:n.532+167G>A
Search 100 bp 5'
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