Canonical Allele Identifier: CA411376868
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960719G>T (hg19) chr22:g.36564672G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564672G>T , CM000684.2:g.36564672G>T GRCh38
NC_000022.10:g.36960719G>T , CM000684.1:g.36960719G>T GRCh37
NC_000022.9:g.35290665G>T NCBI36
NG_031861.1:g.142972C>A
NG_031861.2:g.143187C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.651C>A MANE Select ENSP00000300105.6:p.Tyr217Ter
ENST00000300105.6:c.651C>A ENSP00000300105.6:p.Tyr217Ter
NM_006078.3:c.651C>A NP_006069.1:p.Tyr217Ter
NM_006078.4:c.651C>A NP_006069.1:p.Tyr217Ter
XM_017028531.2:c.393C>A XP_016884020.1:p.Tyr131Ter
NM_001379051.1:c.582C>A NP_001365980.1:p.Tyr194Ter
NM_006078.5:c.651C>A MANE Select NP_006069.1:p.Tyr217Ter
NR_166440.1:n.2017C>A
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