Canonical Allele Identifier: CA2403929659
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564724A= , CM000684.2:g.36564724A= GRCh38
NC_000022.10:g.36960771A= , CM000684.1:g.36960771A= GRCh37
NC_000022.9:g.35290717A= NCBI36
NG_031861.1:g.142920T=
NG_031861.2:g.143135T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.599T= MANE Select ENSP00000300105.6:p.Met200=
ENST00000300105.6:c.599T= ENSP00000300105.6:p.Met200=
NM_006078.3:c.599T= NP_006069.1:p.Met200=
NM_006078.4:c.599T= NP_006069.1:p.Met200=
XM_017028531.2:c.341T= XP_016884020.1:p.Met114=
NM_001379051.1:c.530T= NP_001365980.1:p.Met177=
NM_006078.5:c.599T= MANE Select NP_006069.1:p.Met200=
NR_166440.1:n.1965T=