Canonical Allele Identifier: CA2403929760
Gene: CACNG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564985T= , CM000684.2:g.36564985T= GRCh38
NC_000022.10:g.36961032T= , CM000684.1:g.36961032T= GRCh37
NC_000022.9:g.35290978T= NCBI36
NG_031861.1:g.142659A=
NG_031861.2:g.142874A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-99A= MANE Select ENSP00000300105.6:n.437-99A=
ENST00000300105.6:c.437-99A= ENSP00000300105.6:n.437-99A=
NM_006078.3:c.437-99A= NP_006069.1:n.437-99A=
NM_006078.4:c.437-99A= NP_006069.1:n.437-99A=
XM_017028531.2:c.179-99A= XP_016884020.1:n.179-99A=
NM_001379051.1:c.368-99A= NP_001365980.1:n.368-99A=
NM_006078.5:c.437-99A= MANE Select NP_006069.1:n.437-99A=
NR_166440.1:n.1803-99A=
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