Canonical Allele Identifier: CA2403929701
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564845T= , CM000684.2:g.36564845T= GRCh38
NC_000022.10:g.36960892T= , CM000684.1:g.36960892T= GRCh37
NC_000022.9:g.35290838T= NCBI36
NG_031861.1:g.142799A=
NG_031861.2:g.143014A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.478A= MANE Select ENSP00000300105.6:p.Asn160=
ENST00000300105.6:c.478A= ENSP00000300105.6:p.Asn160=
NM_006078.3:c.478A= NP_006069.1:p.Asn160=
NM_006078.4:c.478A= NP_006069.1:p.Asn160=
XM_017028531.2:c.220A= XP_016884020.1:p.Asn74=
NM_001379051.1:c.409A= NP_001365980.1:p.Asn137=
NM_006078.5:c.478A= MANE Select NP_006069.1:p.Asn160=
NR_166440.1:n.1844A=