Canonical Allele Identifier: CA514475078

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960848G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564801G>A , CM000684.2:g.36564801G>A	GRCh38
NC_000022.10:g.36960848G>A , CM000684.1:g.36960848G>A	GRCh37
NC_000022.9:g.35290794G>A	NCBI36
NG_031861.1:g.142843C>T
NG_031861.2:g.143058C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.522C>T MANE Select	ENSP00000300105.6:p.Tyr174=
ENST00000300105.6:c.522C>T	ENSP00000300105.6:p.Tyr174=
NM_006078.3:c.522C>T	NP_006069.1:p.Tyr174=
NM_006078.4:c.522C>T	NP_006069.1:p.Tyr174=
XM_017028531.2:c.264C>T	XP_016884020.1:p.Tyr88=
NM_001379051.1:c.453C>T	NP_001365980.1:p.Tyr151=
NM_006078.5:c.522C>T MANE Select	NP_006069.1:p.Tyr174=
NR_166440.1:n.1888C>T