Canonical Allele Identifier: CA1023984
Gene: CASQ2 HGNC NCBI

Linked Data

dbSNP Id: rs151250797

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115768314C>A , CM000663.2:g.115768314C>A GRCh38
NC_000001.10:g.116310935C>A , CM000663.1:g.116310935C>A GRCh37
NC_000001.9:g.116112458C>A NCBI36
NG_008802.1:g.5492G>T , LRG_404:g.5492G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000488931.2:c.-49G>T ENSP00000518226.1:n.-49G>T
ENST00000261448.6:c.228G>T MANE Select ENSP00000261448.5:p.Val76=
ENST00000261448.5:c.228G>T ENSP00000261448.5:p.Val76=
NM_001232.3:c.228G>T , LRG_404t1:c.228G>T NP_001223.2:p.Val76=
NM_001232.4:c.228G>T MANE Select NP_001223.2:p.Val76=