Canonical Allele Identifier: CA525631277
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs1397343707
gnomAD v2: 1-116311193-T-C
gnomAD v4: 1-115768572-T-C
MyVariant Identifiers: chr1:g.116311193T>C (hg19) chr1:g.115768572T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768572T>C , CM000663.2:g.115768572T>C GRCh38
NC_000001.10:g.116311193T>C , CM000663.1:g.116311193T>C GRCh37
NC_000001.9:g.116112716T>C NCBI36
NG_008802.1:g.5234A>G , LRG_404:g.5234A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000488931.2:c.-223-84A>G ENSP00000518226.1:n.-223-84A>G
ENST00000261448.6:c.-31A>G MANE Select ENSP00000261448.5:n.-31A>G
ENST00000261448.5:c.-31A>G ENSP00000261448.5:n.-31A>G
NM_001232.3:c.-31A>G , LRG_404t1:c.-31A>G NP_001223.2:n.-31A>G
NM_001232.4:c.-31A>G MANE Select NP_001223.2:n.-31A>G
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