Canonical Allele Identifier: CA411376972
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960733G>C (hg19) chr22:g.36564686G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564686G>C , CM000684.2:g.36564686G>C GRCh38
NC_000022.10:g.36960733G>C , CM000684.1:g.36960733G>C GRCh37
NC_000022.9:g.35290679G>C NCBI36
NG_031861.1:g.142958C>G
NG_031861.2:g.143173C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.637C>G MANE Select ENSP00000300105.6:p.Arg213Gly
ENST00000300105.6:c.637C>G ENSP00000300105.6:p.Arg213Gly
NM_006078.3:c.637C>G NP_006069.1:p.Arg213Gly
NM_006078.4:c.637C>G NP_006069.1:p.Arg213Gly
XM_017028531.2:c.379C>G XP_016884020.1:p.Arg127Gly
NM_001379051.1:c.568C>G NP_001365980.1:p.Arg190Gly
NM_006078.5:c.637C>G MANE Select NP_006069.1:p.Arg213Gly
NR_166440.1:n.2003C>G
Search 100 bp 5'
Search 100 bp 3'