Canonical Allele Identifier: CA2403929751
Gene: CACNG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564972A= , CM000684.2:g.36564972A= GRCh38
NC_000022.10:g.36961019A= , CM000684.1:g.36961019A= GRCh37
NC_000022.9:g.35290965A= NCBI36
NG_031861.1:g.142672T=
NG_031861.2:g.142887T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-86T= MANE Select ENSP00000300105.6:n.437-86T=
ENST00000300105.6:c.437-86T= ENSP00000300105.6:n.437-86T=
NM_006078.3:c.437-86T= NP_006069.1:n.437-86T=
NM_006078.4:c.437-86T= NP_006069.1:n.437-86T=
XM_017028531.2:c.179-86T= XP_016884020.1:n.179-86T=
NM_001379051.1:c.368-86T= NP_001365980.1:n.368-86T=
NM_006078.5:c.437-86T= MANE Select NP_006069.1:n.437-86T=
NR_166440.1:n.1803-86T=
Search 100 bp 5'
Search 100 bp 3'