Canonical Allele Identifier: CA2724384876
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120110368

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648147G>A , CM000673.2:g.69648147G>A GRCh38
NC_000011.9:g.69462915G>A , CM000673.1:g.69462915G>A GRCh37
NC_000011.8:g.69172096G>A NCBI36
NG_007375.1:g.12043G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.723+5G>A MANE Select ENSP00000227507.2:n.723+5G>A
ENST00000227507.2:c.723+5G>A ENSP00000227507.2:n.723+5G>A
ENST00000536559.1:c.*148G>A ENSP00000438482.1:n.*148G>A
ENST00000542367.1:n.186+5G>A
NM_053056.2:c.723+5G>A NP_444284.1:n.723+5G>A
XM_006718653.2:c.747+5G>A XP_006718716.1:n.747+5G>A
NM_053056.3:c.723+5G>A MANE Select NP_444284.1:n.723+5G>A