Canonical Allele Identifier: CA411378369
Gene: CACNG2 HGNC NCBI

Linked Data

gnomAD v4: 22-36564855-G-T
MyVariant Identifiers: chr22:g.36960902G>T (hg19) chr22:g.36564855G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564855G>T , CM000684.2:g.36564855G>T GRCh38
NC_000022.10:g.36960902G>T , CM000684.1:g.36960902G>T GRCh37
NC_000022.9:g.35290848G>T NCBI36
NG_031861.1:g.142789C>A
NG_031861.2:g.143004C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.468C>A MANE Select ENSP00000300105.6:p.Tyr156Ter
ENST00000300105.6:c.468C>A ENSP00000300105.6:p.Tyr156Ter
NM_006078.3:c.468C>A NP_006069.1:p.Tyr156Ter
NM_006078.4:c.468C>A NP_006069.1:p.Tyr156Ter
XM_017028531.2:c.210C>A XP_016884020.1:p.Tyr70Ter
NM_001379051.1:c.399C>A NP_001365980.1:p.Tyr133Ter
NM_006078.5:c.468C>A MANE Select NP_006069.1:p.Tyr156Ter
NR_166440.1:n.1834C>A
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