Canonical Allele Identifier: CA2403929605
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564605T= , CM000684.2:g.36564605T= GRCh38
NC_000022.10:g.36960652T= , CM000684.1:g.36960652T= GRCh37
NC_000022.9:g.35290598T= NCBI36
NG_031861.1:g.143039A=
NG_031861.2:g.143254A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.718A= MANE Select ENSP00000300105.6:p.Ser240=
ENST00000300105.6:c.718A= ENSP00000300105.6:p.Ser240=
NM_006078.3:c.718A= NP_006069.1:p.Ser240=
NM_006078.4:c.718A= NP_006069.1:p.Ser240=
XM_017028531.2:c.460A= XP_016884020.1:p.Ser154=
NM_001379051.1:c.649A= NP_001365980.1:p.Ser217=
NM_006078.5:c.718A= MANE Select NP_006069.1:p.Ser240=
NR_166440.1:n.2084A=