Canonical Allele Identifier: CA2403994168

Gene: CACNG2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36701480C= , CM000684.2:g.36701480C=	GRCh38
NC_000022.10:g.37097525C= , CM000684.1:g.37097525C=	GRCh37
NC_000022.9:g.35427471C=	NCBI36
NG_031861.1:g.6166G=
NG_031861.2:g.6379G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300105.7:c.211+886G= MANE Select	ENSP00000300105.6:n.211+886G=
ENST00000300105.6:c.211+886G=	ENSP00000300105.6:n.211+886G=
NM_006078.3:c.211+886G=	NP_006069.1:n.211+886G=
NM_006078.4:c.211+886G=	NP_006069.1:n.211+886G=
NM_001379051.1:c.142+886G=	NP_001365980.1:n.142+886G=
NM_006078.5:c.211+886G= MANE Select	NP_006069.1:n.211+886G=
NR_166440.1:n.1387+886G=