Canonical Allele Identifier: CA514475131

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960692G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564645G>A , CM000684.2:g.36564645G>A	GRCh38
NC_000022.10:g.36960692G>A , CM000684.1:g.36960692G>A	GRCh37
NC_000022.9:g.35290638G>A	NCBI36
NG_031861.1:g.142999C>T
NG_031861.2:g.143214C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.678C>T MANE Select	ENSP00000300105.6:p.Ile226=
ENST00000300105.6:c.678C>T	ENSP00000300105.6:p.Ile226=
NM_006078.3:c.678C>T	NP_006069.1:p.Ile226=
NM_006078.4:c.678C>T	NP_006069.1:p.Ile226=
XM_017028531.2:c.420C>T	XP_016884020.1:p.Ile140=
NM_001379051.1:c.609C>T	NP_001365980.1:p.Ile203=
NM_006078.5:c.678C>T MANE Select	NP_006069.1:p.Ile226=
NR_166440.1:n.2044C>T