Canonical Allele Identifier: CA2818892107
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36701497G>A , CM000684.2:g.36701497G>A GRCh38
NC_000022.10:g.37097542G>A , CM000684.1:g.37097542G>A GRCh37
NC_000022.9:g.35427488G>A NCBI36
NG_031861.1:g.6149C>T
NG_031861.2:g.6362C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.211+869C>T MANE Select ENSP00000300105.6:n.211+869C>T
ENST00000300105.6:c.211+869C>T ENSP00000300105.6:n.211+869C>T
NM_006078.3:c.211+869C>T NP_006069.1:n.211+869C>T
NM_006078.4:c.211+869C>T NP_006069.1:n.211+869C>T
NM_001379051.1:c.142+869C>T NP_001365980.1:n.142+869C>T
NM_006078.5:c.211+869C>T MANE Select NP_006069.1:n.211+869C>T
NR_166440.1:n.1387+869C>T