Canonical Allele Identifier: CA2724213405

Gene: CCND1

Linked Data

• dbSNP Id: rs987619423

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648232C>G , CM000673.2:g.69648232C>G	GRCh38
NC_000011.9:g.69463000C>G , CM000673.1:g.69463000C>G	GRCh37
NC_000011.8:g.69172181C>G	NCBI36
NG_007375.1:g.12128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+90C>G MANE Select	ENSP00000227507.2:n.723+90C>G
ENST00000227507.2:c.723+90C>G	ENSP00000227507.2:n.723+90C>G
ENST00000536559.1:c.*233C>G	ENSP00000438482.1:n.*233C>G
ENST00000542367.1:n.186+90C>G
NM_053056.2:c.723+90C>G	NP_444284.1:n.723+90C>G
XM_006718653.2:c.747+90C>G	XP_006718716.1:n.747+90C>G
NM_053056.3:c.723+90C>G MANE Select	NP_444284.1:n.723+90C>G