Canonical Allele Identifier: CA2724205571
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs900676385
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647807C>G , CM000673.2:g.69647807C>G GRCh38
NC_000011.9:g.69462575C>G , CM000673.1:g.69462575C>G GRCh37
NC_000011.8:g.69171756C>G NCBI36
NG_007375.1:g.11703C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575-187C>G MANE Select ENSP00000227507.2:n.575-187C>G
ENST00000227507.2:c.575-187C>G ENSP00000227507.2:n.575-187C>G
ENST00000536559.1:c.199-187C>G ENSP00000438482.1:n.199-187C>G
ENST00000545484.1:n.281-187C>G
NM_053056.2:c.575-187C>G NP_444284.1:n.575-187C>G
XM_006718653.2:c.599-187C>G XP_006718716.1:n.599-187C>G
NM_053056.3:c.575-187C>G MANE Select NP_444284.1:n.575-187C>G
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