Canonical Allele Identifier: CA2724289825
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855809832

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648193A>G , CM000673.2:g.69648193A>G GRCh38
NC_000011.9:g.69462961A>G , CM000673.1:g.69462961A>G GRCh37
NC_000011.8:g.69172142A>G NCBI36
NG_007375.1:g.12089A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+51A>G MANE Select ENSP00000227507.2:n.723+51A>G
ENST00000227507.2:c.723+51A>G ENSP00000227507.2:n.723+51A>G
ENST00000536559.1:c.*194A>G ENSP00000438482.1:n.*194A>G
ENST00000542367.1:n.186+51A>G
NM_053056.2:c.723+51A>G NP_444284.1:n.723+51A>G
XM_006718653.2:c.747+51A>G XP_006718716.1:n.747+51A>G
NM_053056.3:c.723+51A>G MANE Select NP_444284.1:n.723+51A>G