Canonical Allele Identifier: CA2403929682
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564807A= , CM000684.2:g.36564807A= GRCh38
NC_000022.10:g.36960854A= , CM000684.1:g.36960854A= GRCh37
NC_000022.9:g.35290800A= NCBI36
NG_031861.1:g.142837T=
NG_031861.2:g.143052T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.516T= MANE Select ENSP00000300105.6:p.Asn172=
ENST00000300105.6:c.516T= ENSP00000300105.6:p.Asn172=
NM_006078.3:c.516T= NP_006069.1:p.Asn172=
NM_006078.4:c.516T= NP_006069.1:p.Asn172=
XM_017028531.2:c.258T= XP_016884020.1:p.Asn86=
NM_001379051.1:c.447T= NP_001365980.1:p.Asn149=
NM_006078.5:c.516T= MANE Select NP_006069.1:p.Asn172=
NR_166440.1:n.1882T=