Canonical Allele Identifier: CA411378031
Gene: CACNG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564822G>C , CM000684.2:g.36564822G>C GRCh38
NC_000022.10:g.36960869G>C , CM000684.1:g.36960869G>C GRCh37
NC_000022.9:g.35290815G>C NCBI36
NG_031861.1:g.142822C>G
NG_031861.2:g.143037C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.501C>G MANE Select ENSP00000300105.6:p.Ser167Arg
ENST00000300105.6:c.501C>G ENSP00000300105.6:p.Ser167Arg
NM_006078.3:c.501C>G NP_006069.1:p.Ser167Arg
NM_006078.4:c.501C>G NP_006069.1:p.Ser167Arg
XM_017028531.2:c.243C>G XP_016884020.1:p.Ser81Arg
NM_001379051.1:c.432C>G NP_001365980.1:p.Ser144Arg
NM_006078.5:c.501C>G MANE Select NP_006069.1:p.Ser167Arg
NR_166440.1:n.1867C>G