Canonical Allele Identifier: CA2614780007
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120110572
gnomAD v4: 11-69648169-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648169C>A , CM000673.2:g.69648169C>A GRCh38
NC_000011.9:g.69462937C>A , CM000673.1:g.69462937C>A GRCh37
NC_000011.8:g.69172118C>A NCBI36
NG_007375.1:g.12065C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+27C>A MANE Select ENSP00000227507.2:n.723+27C>A
ENST00000227507.2:c.723+27C>A ENSP00000227507.2:n.723+27C>A
ENST00000536559.1:c.*170C>A ENSP00000438482.1:n.*170C>A
ENST00000542367.1:n.186+27C>A
NM_053056.2:c.723+27C>A NP_444284.1:n.723+27C>A
XM_006718653.2:c.747+27C>A XP_006718716.1:n.747+27C>A
NM_053056.3:c.723+27C>A MANE Select NP_444284.1:n.723+27C>A
Search 100 bp 5'
Search 100 bp 3'