Canonical Allele Identifier: CA514475086
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960653G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564606G>T , CM000684.2:g.36564606G>T GRCh38
NC_000022.10:g.36960653G>T , CM000684.1:g.36960653G>T GRCh37
NC_000022.9:g.35290599G>T NCBI36
NG_031861.1:g.143038C>A
NG_031861.2:g.143253C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.717C>A MANE Select ENSP00000300105.6:p.Ser239=
ENST00000300105.6:c.717C>A ENSP00000300105.6:p.Ser239=
NM_006078.3:c.717C>A NP_006069.1:p.Ser239=
NM_006078.4:c.717C>A NP_006069.1:p.Ser239=
XM_017028531.2:c.459C>A XP_016884020.1:p.Ser153=
NM_001379051.1:c.648C>A NP_001365980.1:p.Ser216=
NM_006078.5:c.717C>A MANE Select NP_006069.1:p.Ser239=
NR_166440.1:n.2083C>A
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