Canonical Allele Identifier: CA2724201693
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs753117077
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648187G>C , CM000673.2:g.69648187G>C GRCh38
NC_000011.9:g.69462955G>C , CM000673.1:g.69462955G>C GRCh37
NC_000011.8:g.69172136G>C NCBI36
NG_007375.1:g.12083G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+45G>C MANE Select ENSP00000227507.2:n.723+45G>C
ENST00000227507.2:c.723+45G>C ENSP00000227507.2:n.723+45G>C
ENST00000536559.1:c.*188G>C ENSP00000438482.1:n.*188G>C
ENST00000542367.1:n.186+45G>C
NM_053056.2:c.723+45G>C NP_444284.1:n.723+45G>C
XM_006718653.2:c.747+45G>C XP_006718716.1:n.747+45G>C
NM_053056.3:c.723+45G>C MANE Select NP_444284.1:n.723+45G>C
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