Canonical Allele Identifier: CA411377625
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960825A>T (hg19) chr22:g.36564778A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564778A>T , CM000684.2:g.36564778A>T GRCh38
NC_000022.10:g.36960825A>T , CM000684.1:g.36960825A>T GRCh37
NC_000022.9:g.35290771A>T NCBI36
NG_031861.1:g.142866T>A
NG_031861.2:g.143081T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.545T>A MANE Select ENSP00000300105.6:p.Phe182Tyr
ENST00000300105.6:c.545T>A ENSP00000300105.6:p.Phe182Tyr
NM_006078.3:c.545T>A NP_006069.1:p.Phe182Tyr
NM_006078.4:c.545T>A NP_006069.1:p.Phe182Tyr
XM_017028531.2:c.287T>A XP_016884020.1:p.Phe96Tyr
NM_001379051.1:c.476T>A NP_001365980.1:p.Phe159Tyr
NM_006078.5:c.545T>A MANE Select NP_006069.1:p.Phe182Tyr
NR_166440.1:n.1911T>A
Search 100 bp 5'
Search 100 bp 3'