Canonical Allele Identifier: CA411378619

Gene: CACNG2

Linked Data

• MyVariant Identifiers: chr22:g.36960935T>G (hg19) ; chr22:g.36564888T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564888T>G , CM000684.2:g.36564888T>G	GRCh38
NC_000022.10:g.36960935T>G , CM000684.1:g.36960935T>G	GRCh37
NC_000022.9:g.35290881T>G	NCBI36
NG_031861.1:g.142756A>C
NG_031861.2:g.142971A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-2A>C MANE Select	ENSP00000300105.6:n.437-2A>C
ENST00000300105.6:c.437-2A>C	ENSP00000300105.6:n.437-2A>C
NM_006078.3:c.437-2A>C	NP_006069.1:n.437-2A>C
NM_006078.4:c.437-2A>C	NP_006069.1:n.437-2A>C
XM_017028531.2:c.179-2A>C	XP_016884020.1:n.179-2A>C
NM_001379051.1:c.368-2A>C	NP_001365980.1:n.368-2A>C
NM_006078.5:c.437-2A>C MANE Select	NP_006069.1:n.437-2A>C
NR_166440.1:n.1803-2A>C