Canonical Allele Identifier: CA2403929647
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564694G= , CM000684.2:g.36564694G= GRCh38
NC_000022.10:g.36960741G= , CM000684.1:g.36960741G= GRCh37
NC_000022.9:g.35290687G= NCBI36
NG_031861.1:g.142950C=
NG_031861.2:g.143165C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.629C= MANE Select ENSP00000300105.6:p.Ala210=
ENST00000300105.6:c.629C= ENSP00000300105.6:p.Ala210=
NM_006078.3:c.629C= NP_006069.1:p.Ala210=
NM_006078.4:c.629C= NP_006069.1:p.Ala210=
XM_017028531.2:c.371C= XP_016884020.1:p.Ala124=
NM_001379051.1:c.560C= NP_001365980.1:p.Ala187=
NM_006078.5:c.629C= MANE Select NP_006069.1:p.Ala210=
NR_166440.1:n.1995C=