Canonical Allele Identifier: CA2403929633
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564675G= , CM000684.2:g.36564675G= GRCh38
NC_000022.10:g.36960722G= , CM000684.1:g.36960722G= GRCh37
NC_000022.9:g.35290668G= NCBI36
NG_031861.1:g.142969C=
NG_031861.2:g.143184C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.648C= MANE Select ENSP00000300105.6:p.Asp216=
ENST00000300105.6:c.648C= ENSP00000300105.6:p.Asp216=
NM_006078.3:c.648C= NP_006069.1:p.Asp216=
NM_006078.4:c.648C= NP_006069.1:p.Asp216=
XM_017028531.2:c.390C= XP_016884020.1:p.Asp130=
NM_001379051.1:c.579C= NP_001365980.1:p.Asp193=
NM_006078.5:c.648C= MANE Select NP_006069.1:p.Asp216=
NR_166440.1:n.2014C=