Canonical Allele Identifier: CA514475167

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960917A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564870A>G , CM000684.2:g.36564870A>G	GRCh38
NC_000022.10:g.36960917A>G , CM000684.1:g.36960917A>G	GRCh37
NC_000022.9:g.35290863A>G	NCBI36
NG_031861.1:g.142774T>C
NG_031861.2:g.142989T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.453T>C MANE Select	ENSP00000300105.6:p.Ile151=
ENST00000300105.6:c.453T>C	ENSP00000300105.6:p.Ile151=
NM_006078.3:c.453T>C	NP_006069.1:p.Ile151=
NM_006078.4:c.453T>C	NP_006069.1:p.Ile151=
XM_017028531.2:c.195T>C	XP_016884020.1:p.Ile65=
NM_001379051.1:c.384T>C	NP_001365980.1:p.Ile128=
NM_006078.5:c.453T>C MANE Select	NP_006069.1:p.Ile151=
NR_166440.1:n.1819T>C