Canonical Allele Identifier: CA2724289818

Gene: CCND1

Linked Data

• dbSNP Id: rs1855809781

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648191A>T , CM000673.2:g.69648191A>T	GRCh38
NC_000011.9:g.69462959A>T , CM000673.1:g.69462959A>T	GRCh37
NC_000011.8:g.69172140A>T	NCBI36
NG_007375.1:g.12087A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+49A>T MANE Select	ENSP00000227507.2:n.723+49A>T
ENST00000227507.2:c.723+49A>T	ENSP00000227507.2:n.723+49A>T
ENST00000536559.1:c.*192A>T	ENSP00000438482.1:n.*192A>T
ENST00000542367.1:n.186+49A>T
NM_053056.2:c.723+49A>T	NP_444284.1:n.723+49A>T
XM_006718653.2:c.747+49A>T	XP_006718716.1:n.747+49A>T
NM_053056.3:c.723+49A>T MANE Select	NP_444284.1:n.723+49A>T