Canonical Allele Identifier: CA2403929758
Gene: CACNG2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564979C= , CM000684.2:g.36564979C= GRCh38
NC_000022.10:g.36961026C= , CM000684.1:g.36961026C= GRCh37
NC_000022.9:g.35290972C= NCBI36
NG_031861.1:g.142665G=
NG_031861.2:g.142880G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-93G= MANE Select ENSP00000300105.6:n.437-93G=
ENST00000300105.6:c.437-93G= ENSP00000300105.6:n.437-93G=
NM_006078.3:c.437-93G= NP_006069.1:n.437-93G=
NM_006078.4:c.437-93G= NP_006069.1:n.437-93G=
XM_017028531.2:c.179-93G= XP_016884020.1:n.179-93G=
NM_001379051.1:c.368-93G= NP_001365980.1:n.368-93G=
NM_006078.5:c.437-93G= MANE Select NP_006069.1:n.437-93G=
NR_166440.1:n.1803-93G=
Search 100 bp 5'
Search 100 bp 3'