Canonical Allele Identifier: CA411377008
Gene: CACNG2 HGNC NCBI

Linked Data

gnomAD v4: 22-36564695-C-T
MyVariant Identifiers: chr22:g.36960742C>T (hg19) chr22:g.36564695C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564695C>T , CM000684.2:g.36564695C>T GRCh38
NC_000022.10:g.36960742C>T , CM000684.1:g.36960742C>T GRCh37
NC_000022.9:g.35290688C>T NCBI36
NG_031861.1:g.142949G>A
NG_031861.2:g.143164G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.628G>A MANE Select ENSP00000300105.6:p.Ala210Thr
ENST00000300105.6:c.628G>A ENSP00000300105.6:p.Ala210Thr
NM_006078.3:c.628G>A NP_006069.1:p.Ala210Thr
NM_006078.4:c.628G>A NP_006069.1:p.Ala210Thr
XM_017028531.2:c.370G>A XP_016884020.1:p.Ala124Thr
NM_001379051.1:c.559G>A NP_001365980.1:p.Ala187Thr
NM_006078.5:c.628G>A MANE Select NP_006069.1:p.Ala210Thr
NR_166440.1:n.1994G>A
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