Canonical Allele Identifier: CA939231215
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855834230
gnomAD v3: 11-69649956-A-G
gnomAD v4: 11-69649956-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69649956A>G , CM000673.2:g.69649956A>G GRCh38
NC_000011.9:g.69464724A>G , CM000673.1:g.69464724A>G GRCh37
NC_000011.8:g.69173905A>G NCBI36
NG_007375.1:g.13852A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.724-1162A>G MANE Select ENSP00000227507.2:n.724-1162A>G
ENST00000227507.2:c.724-1162A>G ENSP00000227507.2:n.724-1162A>G
ENST00000542367.1:n.187-1162A>G
NM_053056.2:c.724-1162A>G NP_444284.1:n.724-1162A>G
XM_006718653.2:c.748-1162A>G XP_006718716.1:n.748-1162A>G
NM_053056.3:c.724-1162A>G MANE Select NP_444284.1:n.724-1162A>G
Search 100 bp 5'
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