Canonical Allele Identifier: CA2403929768
Gene: CACNG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36565005G= , CM000684.2:g.36565005G= GRCh38
NC_000022.10:g.36961052G= , CM000684.1:g.36961052G= GRCh37
NC_000022.9:g.35290998G= NCBI36
NG_031861.1:g.142639C=
NG_031861.2:g.142854C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-119C= MANE Select ENSP00000300105.6:n.437-119C=
ENST00000300105.6:c.437-119C= ENSP00000300105.6:n.437-119C=
NM_006078.3:c.437-119C= NP_006069.1:n.437-119C=
NM_006078.4:c.437-119C= NP_006069.1:n.437-119C=
XM_017028531.2:c.179-119C= XP_016884020.1:n.179-119C=
NM_001379051.1:c.368-119C= NP_001365980.1:n.368-119C=
NM_006078.5:c.437-119C= MANE Select NP_006069.1:n.437-119C=
NR_166440.1:n.1803-119C=
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