Canonical Allele Identifier: CA2577703846
Gene: CACNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564946A>G , CM000684.2:g.36564946A>G GRCh38
NC_000022.10:g.36960993A>G , CM000684.1:g.36960993A>G GRCh37
NC_000022.9:g.35290939A>G NCBI36
NG_031861.1:g.142698T>C
NG_031861.2:g.142913T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-60T>C MANE Select ENSP00000300105.6:n.437-60T>C
ENST00000300105.6:c.437-60T>C ENSP00000300105.6:n.437-60T>C
NM_006078.3:c.437-60T>C NP_006069.1:n.437-60T>C
NM_006078.4:c.437-60T>C NP_006069.1:n.437-60T>C
XM_017028531.2:c.179-60T>C XP_016884020.1:n.179-60T>C
NM_001379051.1:c.368-60T>C NP_001365980.1:n.368-60T>C
NM_006078.5:c.437-60T>C MANE Select NP_006069.1:n.437-60T>C
NR_166440.1:n.1803-60T>C