Canonical Allele Identifier: CA411378442
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960915C>T (hg19) chr22:g.36564868C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564868C>T , CM000684.2:g.36564868C>T GRCh38
NC_000022.10:g.36960915C>T , CM000684.1:g.36960915C>T GRCh37
NC_000022.9:g.35290861C>T NCBI36
NG_031861.1:g.142776G>A
NG_031861.2:g.142991G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.455G>A MANE Select ENSP00000300105.6:p.Gly152Asp
ENST00000300105.6:c.455G>A ENSP00000300105.6:p.Gly152Asp
NM_006078.3:c.455G>A NP_006069.1:p.Gly152Asp
NM_006078.4:c.455G>A NP_006069.1:p.Gly152Asp
XM_017028531.2:c.197G>A XP_016884020.1:p.Gly66Asp
NM_001379051.1:c.386G>A NP_001365980.1:p.Gly129Asp
NM_006078.5:c.455G>A MANE Select NP_006069.1:p.Gly152Asp
NR_166440.1:n.1821G>A
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