Canonical Allele Identifier: CA411378408

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960908T>C (hg19) ; chr22:g.36564861T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564861T>C , CM000684.2:g.36564861T>C	GRCh38
NC_000022.10:g.36960908T>C , CM000684.1:g.36960908T>C	GRCh37
NC_000022.9:g.35290854T>C	NCBI36
NG_031861.1:g.142783A>G
NG_031861.2:g.142998A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.462A>G MANE Select	ENSP00000300105.6:p.Ile154Met
ENST00000300105.6:c.462A>G	ENSP00000300105.6:p.Ile154Met
NM_006078.3:c.462A>G	NP_006069.1:p.Ile154Met
NM_006078.4:c.462A>G	NP_006069.1:p.Ile154Met
XM_017028531.2:c.204A>G	XP_016884020.1:p.Ile68Met
NM_001379051.1:c.393A>G	NP_001365980.1:p.Ile131Met
NM_006078.5:c.462A>G MANE Select	NP_006069.1:p.Ile154Met
NR_166440.1:n.1828A>G