Canonical Allele Identifier: CA2403929707
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564872T= , CM000684.2:g.36564872T= GRCh38
NC_000022.10:g.36960919T= , CM000684.1:g.36960919T= GRCh37
NC_000022.9:g.35290865T= NCBI36
NG_031861.1:g.142772A=
NG_031861.2:g.142987A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.451A= MANE Select ENSP00000300105.6:p.Ile151=
ENST00000300105.6:c.451A= ENSP00000300105.6:p.Ile151=
NM_006078.3:c.451A= NP_006069.1:p.Ile151=
NM_006078.4:c.451A= NP_006069.1:p.Ile151=
XM_017028531.2:c.193A= XP_016884020.1:p.Ile65=
NM_001379051.1:c.382A= NP_001365980.1:p.Ile128=
NM_006078.5:c.451A= MANE Select NP_006069.1:p.Ile151=
NR_166440.1:n.1817A=