Canonical Allele Identifier: CA2724227893

Gene: CCND1

Linked Data

• dbSNP Id: rs1266460935

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647747C>T , CM000673.2:g.69647747C>T	GRCh38
NC_000011.9:g.69462515C>T , CM000673.1:g.69462515C>T	GRCh37
NC_000011.8:g.69171696C>T	NCBI36
NG_007375.1:g.11643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.575-247C>T MANE Select	ENSP00000227507.2:n.575-247C>T
ENST00000227507.2:c.575-247C>T	ENSP00000227507.2:n.575-247C>T
ENST00000536559.1:c.199-247C>T	ENSP00000438482.1:n.199-247C>T
ENST00000545484.1:n.281-247C>T
NM_053056.2:c.575-247C>T	NP_444284.1:n.575-247C>T
XM_006718653.2:c.599-247C>T	XP_006718716.1:n.599-247C>T
NM_053056.3:c.575-247C>T MANE Select	NP_444284.1:n.575-247C>T