Canonical Allele Identifier: CA2724290310
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855834697
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69649994C>T , CM000673.2:g.69649994C>T GRCh38
NC_000011.9:g.69464762C>T , CM000673.1:g.69464762C>T GRCh37
NC_000011.8:g.69173943C>T NCBI36
NG_007375.1:g.13890C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.724-1124C>T MANE Select ENSP00000227507.2:n.724-1124C>T
ENST00000227507.2:c.724-1124C>T ENSP00000227507.2:n.724-1124C>T
ENST00000542367.1:n.187-1124C>T
NM_053056.2:c.724-1124C>T NP_444284.1:n.724-1124C>T
XM_006718653.2:c.748-1124C>T XP_006718716.1:n.748-1124C>T
NM_053056.3:c.724-1124C>T MANE Select NP_444284.1:n.724-1124C>T
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