Canonical Allele Identifier: CA752883903
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs941406909
MyVariant Identifiers: chr22:g.37097526G>C (hg19) chr22:g.36701481G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36701481G>C , CM000684.2:g.36701481G>C GRCh38
NC_000022.10:g.37097526G>C , CM000684.1:g.37097526G>C GRCh37
NC_000022.9:g.35427472G>C NCBI36
NG_031861.1:g.6165C>G
NG_031861.2:g.6378C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.211+885C>G MANE Select ENSP00000300105.6:n.211+885C>G
ENST00000300105.6:c.211+885C>G ENSP00000300105.6:n.211+885C>G
NM_006078.3:c.211+885C>G NP_006069.1:n.211+885C>G
NM_006078.4:c.211+885C>G NP_006069.1:n.211+885C>G
NM_001379051.1:c.142+885C>G NP_001365980.1:n.142+885C>G
NM_006078.5:c.211+885C>G MANE Select NP_006069.1:n.211+885C>G
NR_166440.1:n.1387+885C>G
Search 100 bp 5'
Search 100 bp 3'