Canonical Allele Identifier: CA411376726

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960700T>A (hg19) ; chr22:g.36564653T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564653T>A , CM000684.2:g.36564653T>A	GRCh38
NC_000022.10:g.36960700T>A , CM000684.1:g.36960700T>A	GRCh37
NC_000022.9:g.35290646T>A	NCBI36
NG_031861.1:g.142991A>T
NG_031861.2:g.143206A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.670A>T MANE Select	ENSP00000300105.6:p.Thr224Ser
ENST00000300105.6:c.670A>T	ENSP00000300105.6:p.Thr224Ser
NM_006078.3:c.670A>T	NP_006069.1:p.Thr224Ser
NM_006078.4:c.670A>T	NP_006069.1:p.Thr224Ser
XM_017028531.2:c.412A>T	XP_016884020.1:p.Thr138Ser
NM_001379051.1:c.601A>T	NP_001365980.1:p.Thr201Ser
NM_006078.5:c.670A>T MANE Select	NP_006069.1:p.Thr224Ser
NR_166440.1:n.2036A>T