Canonical Allele Identifier: CA6156262
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs770661706

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648091G>C , CM000673.2:g.69648091G>C GRCh38
NC_000011.9:g.69462859G>C , CM000673.1:g.69462859G>C GRCh37
NC_000011.8:g.69172040G>C NCBI36
NG_007375.1:g.11987G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.672G>C MANE Select ENSP00000227507.2:p.Leu224=
ENST00000227507.2:c.672G>C ENSP00000227507.2:p.Leu224=
ENST00000536559.1:c.*92G>C ENSP00000438482.1:n.*92G>C
ENST00000542367.1:n.135G>C
ENST00000545484.1:n.378G>C
NM_053056.2:c.672G>C NP_444284.1:p.Leu224=
XM_006718653.2:c.696G>C XP_006718716.1:p.Leu232=
NM_053056.3:c.672G>C MANE Select NP_444284.1:p.Leu224=