Canonical Allele Identifier: CA2403994167
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1186146424
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36701477C>A , CM000684.2:g.36701477C>A GRCh38
NC_000022.10:g.37097522C>A , CM000684.1:g.37097522C>A GRCh37
NC_000022.9:g.35427468C>A NCBI36
NG_031861.1:g.6169G>T
NG_031861.2:g.6382G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.211+889G>T MANE Select ENSP00000300105.6:n.211+889G>T
ENST00000300105.6:c.211+889G>T ENSP00000300105.6:n.211+889G>T
NM_006078.3:c.211+889G>T NP_006069.1:n.211+889G>T
NM_006078.4:c.211+889G>T NP_006069.1:n.211+889G>T
NM_001379051.1:c.142+889G>T NP_001365980.1:n.142+889G>T
NM_006078.5:c.211+889G>T MANE Select NP_006069.1:n.211+889G>T
NR_166440.1:n.1387+889G>T
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