Canonical Allele Identifier: CA2403929643
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564689C= , CM000684.2:g.36564689C= GRCh38
NC_000022.10:g.36960736C= , CM000684.1:g.36960736C= GRCh37
NC_000022.9:g.35290682C= NCBI36
NG_031861.1:g.142955G=
NG_031861.2:g.143170G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.634G= MANE Select ENSP00000300105.6:p.Ala212=
ENST00000300105.6:c.634G= ENSP00000300105.6:p.Ala212=
NM_006078.3:c.634G= NP_006069.1:p.Ala212=
NM_006078.4:c.634G= NP_006069.1:p.Ala212=
XM_017028531.2:c.376G= XP_016884020.1:p.Ala126=
NM_001379051.1:c.565G= NP_001365980.1:p.Ala189=
NM_006078.5:c.634G= MANE Select NP_006069.1:p.Ala212=
NR_166440.1:n.2000G=