Canonical Allele Identifier: CA514475159
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs765451812
MyVariant Identifiers: chr22:g.36960911G>T (hg19) chr22:g.36564864G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564864G>T , CM000684.2:g.36564864G>T GRCh38
NC_000022.10:g.36960911G>T , CM000684.1:g.36960911G>T GRCh37
NC_000022.9:g.35290857G>T NCBI36
NG_031861.1:g.142780C>A
NG_031861.2:g.142995C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.459C>A MANE Select ENSP00000300105.6:p.Ile153=
ENST00000300105.6:c.459C>A ENSP00000300105.6:p.Ile153=
NM_006078.3:c.459C>A NP_006069.1:p.Ile153=
NM_006078.4:c.459C>A NP_006069.1:p.Ile153=
XM_017028531.2:c.201C>A XP_016884020.1:p.Ile67=
NM_001379051.1:c.390C>A NP_001365980.1:p.Ile130=
NM_006078.5:c.459C>A MANE Select NP_006069.1:p.Ile153=
NR_166440.1:n.1825C>A
Search 100 bp 5'
Search 100 bp 3'