Canonical Allele Identifier: CA2403994166
Gene: CACNG2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.211+889G= MANE Select ENSP00000300105.6:n.211+889G=
ENST00000300105.6:c.211+889G= ENSP00000300105.6:n.211+889G=
NM_006078.3:c.211+889G= NP_006069.1:n.211+889G=
NM_006078.4:c.211+889G= NP_006069.1:n.211+889G=
NM_001379051.1:c.142+889G= NP_001365980.1:n.142+889G=
NM_006078.5:c.211+889G= MANE Select NP_006069.1:n.211+889G=
NR_166440.1:n.1387+889G=
Search 100 bp 5'
Search 100 bp 3'