Canonical Allele Identifier: CA14271755
Gene: ATP2C2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10514604

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84412778C>G , CM000678.2:g.84412778C>G GRCh38
NC_000016.9:g.84446384C>G , CM000678.1:g.84446384C>G GRCh37
NC_000016.8:g.83003885C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001286527.2:c.515+2013C>G VV NP_001273456.2:p.=
NM_001291454.1:c.62+2175C>G VV NP_001278383.1:p.=
NM_014861.3:c.515+2013C>G VV NP_055676.3:p.=
XM_011523486.1:c.446+2013C>G XP_011521788.1:p.=
XM_011523486.2:c.446+2013C>G
XR_001752045.1:n.608+2013C>G
ENST00000262429.8:c.515+2013C>G ENSP00000262429.4:p.=
ENST00000416219.6:c.515+2013C>G ENSP00000397925.2:p.=
ENST00000420010.6:n.188+2175C>G
ENST00000565546.5:n.250+2013C>G
ENST00000565631.5:n.1006+2013C>G
ENST00000565927.1:n.504+2013C>G
ENST00000569207.5:n.237+2013C>G