Canonical Allele Identifier: CA2403994163
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36701470C= , CM000684.2:g.36701470C= GRCh38
NC_000022.10:g.37097515C= , CM000684.1:g.37097515C= GRCh37
NC_000022.9:g.35427461C= NCBI36
NG_031861.1:g.6176G=
NG_031861.2:g.6389G=

Transcript Alleles

HGVS Amino-acid change
ENST00000300105.7:c.211+896G= MANE Select ENSP00000300105.6:n.211+896G=
ENST00000300105.6:c.211+896G= ENSP00000300105.6:n.211+896G=
NM_006078.3:c.211+896G= NP_006069.1:n.211+896G=
NM_006078.4:c.211+896G= NP_006069.1:n.211+896G=
NM_001379051.1:c.142+896G= NP_001365980.1:n.142+896G=
NM_006078.5:c.211+896G= MANE Select NP_006069.1:n.211+896G=
NR_166440.1:n.1387+896G=