Canonical Allele Identifier: CA2403994169
Gene: CACNG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36701481G= , CM000684.2:g.36701481G= GRCh38
NC_000022.10:g.37097526G= , CM000684.1:g.37097526G= GRCh37
NC_000022.9:g.35427472G= NCBI36
NG_031861.1:g.6165C=
NG_031861.2:g.6378C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300105.7:c.211+885C= MANE Select ENSP00000300105.6:n.211+885C=
ENST00000300105.6:c.211+885C= ENSP00000300105.6:n.211+885C=
NM_006078.3:c.211+885C= NP_006069.1:n.211+885C=
NM_006078.4:c.211+885C= NP_006069.1:n.211+885C=
NM_001379051.1:c.142+885C= NP_001365980.1:n.142+885C=
NM_006078.5:c.211+885C= MANE Select NP_006069.1:n.211+885C=
NR_166440.1:n.1387+885C=
Search 100 bp 5'
Search 100 bp 3'