Canonical Allele Identifier: CA2724384621

Gene: CCND1

Linked Data

• dbSNP Id: rs2120107856

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69647905C>T , CM000673.2:g.69647905C>T	GRCh38
NC_000011.9:g.69462673C>T , CM000673.1:g.69462673C>T	GRCh37
NC_000011.8:g.69171854C>T	NCBI36
NG_007375.1:g.11801C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.575-89C>T MANE Select	ENSP00000227507.2:n.575-89C>T
ENST00000227507.2:c.575-89C>T	ENSP00000227507.2:n.575-89C>T
ENST00000536559.1:c.199-89C>T	ENSP00000438482.1:n.199-89C>T
ENST00000545484.1:n.281-89C>T
NM_053056.2:c.575-89C>T	NP_444284.1:n.575-89C>T
XM_006718653.2:c.599-89C>T	XP_006718716.1:n.599-89C>T
NM_053056.3:c.575-89C>T MANE Select	NP_444284.1:n.575-89C>T