Canonical Allele Identifier: CA2403929604
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564600C= , CM000684.2:g.36564600C= GRCh38
NC_000022.10:g.36960647C= , CM000684.1:g.36960647C= GRCh37
NC_000022.9:g.35290593C= NCBI36
NG_031861.1:g.143044G=
NG_031861.2:g.143259G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.723G= MANE Select ENSP00000300105.6:p.Ser241=
ENST00000300105.6:c.723G= ENSP00000300105.6:p.Ser241=
NM_006078.3:c.723G= NP_006069.1:p.Ser241=
NM_006078.4:c.723G= NP_006069.1:p.Ser241=
XM_017028531.2:c.465G= XP_016884020.1:p.Ser155=
NM_001379051.1:c.654G= NP_001365980.1:p.Ser218=
NM_006078.5:c.723G= MANE Select NP_006069.1:p.Ser241=
NR_166440.1:n.2089G=