Canonical Allele Identifier: CA514475202
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1898960633
gnomAD v3: 22-36564702-C-T
gnomAD v4: 22-36564702-C-T
MyVariant Identifiers: chr22:g.36960749C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564702C>T , CM000684.2:g.36564702C>T GRCh38
NC_000022.10:g.36960749C>T , CM000684.1:g.36960749C>T GRCh37
NC_000022.9:g.35290695C>T NCBI36
NG_031861.1:g.142942G>A
NG_031861.2:g.143157G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.621G>A MANE Select ENSP00000300105.6:p.Gln207=
ENST00000300105.6:c.621G>A ENSP00000300105.6:p.Gln207=
NM_006078.3:c.621G>A NP_006069.1:p.Gln207=
NM_006078.4:c.621G>A NP_006069.1:p.Gln207=
XM_017028531.2:c.363G>A XP_016884020.1:p.Gln121=
NM_001379051.1:c.552G>A NP_001365980.1:p.Gln184=
NM_006078.5:c.621G>A MANE Select NP_006069.1:p.Gln207=
NR_166440.1:n.1987G>A
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