Canonical Allele Identifier: CA2403994157
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36701460A= , CM000684.2:g.36701460A= GRCh38
NC_000022.10:g.37097505A= , CM000684.1:g.37097505A= GRCh37
NC_000022.9:g.35427451A= NCBI36
NG_031861.1:g.6186T=
NG_031861.2:g.6399T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.211+906T= MANE Select ENSP00000300105.6:n.211+906T=
ENST00000300105.6:c.211+906T= ENSP00000300105.6:n.211+906T=
NM_006078.3:c.211+906T= NP_006069.1:n.211+906T=
NM_006078.4:c.211+906T= NP_006069.1:n.211+906T=
NM_001379051.1:c.142+906T= NP_001365980.1:n.142+906T=
NM_006078.5:c.211+906T= MANE Select NP_006069.1:n.211+906T=
NR_166440.1:n.1387+906T=