Canonical Allele Identifier: CA2403929736
Gene: CACNG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564924G= , CM000684.2:g.36564924G= GRCh38
NC_000022.10:g.36960971G= , CM000684.1:g.36960971G= GRCh37
NC_000022.9:g.35290917G= NCBI36
NG_031861.1:g.142720C=
NG_031861.2:g.142935C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-38C= MANE Select ENSP00000300105.6:n.437-38C=
ENST00000300105.6:c.437-38C= ENSP00000300105.6:n.437-38C=
NM_006078.3:c.437-38C= NP_006069.1:n.437-38C=
NM_006078.4:c.437-38C= NP_006069.1:n.437-38C=
XM_017028531.2:c.179-38C= XP_016884020.1:n.179-38C=
NM_001379051.1:c.368-38C= NP_001365980.1:n.368-38C=
NM_006078.5:c.437-38C= MANE Select NP_006069.1:n.437-38C=
NR_166440.1:n.1803-38C=
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