Canonical Allele Identifier: CA411377108
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960756T>C (hg19) chr22:g.36564709T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564709T>C , CM000684.2:g.36564709T>C GRCh38
NC_000022.10:g.36960756T>C , CM000684.1:g.36960756T>C GRCh37
NC_000022.9:g.35290702T>C NCBI36
NG_031861.1:g.142935A>G
NG_031861.2:g.143150A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.614A>G MANE Select ENSP00000300105.6:p.His205Arg
ENST00000300105.6:c.614A>G ENSP00000300105.6:p.His205Arg
NM_006078.3:c.614A>G NP_006069.1:p.His205Arg
NM_006078.4:c.614A>G NP_006069.1:p.His205Arg
XM_017028531.2:c.356A>G XP_016884020.1:p.His119Arg
NM_001379051.1:c.545A>G NP_001365980.1:p.His182Arg
NM_006078.5:c.614A>G MANE Select NP_006069.1:p.His205Arg
NR_166440.1:n.1980A>G
Search 100 bp 5'
Search 100 bp 3'