Canonical Allele Identifier: CA411377475
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960804A>C (hg19) chr22:g.36564757A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564757A>C , CM000684.2:g.36564757A>C GRCh38
NC_000022.10:g.36960804A>C , CM000684.1:g.36960804A>C GRCh37
NC_000022.9:g.35290750A>C NCBI36
NG_031861.1:g.142887T>G
NG_031861.2:g.143102T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.566T>G MANE Select ENSP00000300105.6:p.Ile189Ser
ENST00000300105.6:c.566T>G ENSP00000300105.6:p.Ile189Ser
NM_006078.3:c.566T>G NP_006069.1:p.Ile189Ser
NM_006078.4:c.566T>G NP_006069.1:p.Ile189Ser
XM_017028531.2:c.308T>G XP_016884020.1:p.Ile103Ser
NM_001379051.1:c.497T>G NP_001365980.1:p.Ile166Ser
NM_006078.5:c.566T>G MANE Select NP_006069.1:p.Ile189Ser
NR_166440.1:n.1932T>G
Search 100 bp 5'
Search 100 bp 3'