Canonical Allele Identifier: CA2724384729
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120108386
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647965G>C , CM000673.2:g.69647965G>C GRCh38
NC_000011.9:g.69462733G>C , CM000673.1:g.69462733G>C GRCh37
NC_000011.8:g.69171914G>C NCBI36
NG_007375.1:g.11861G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575-29G>C MANE Select ENSP00000227507.2:n.575-29G>C
ENST00000227507.2:c.575-29G>C ENSP00000227507.2:n.575-29G>C
ENST00000536559.1:c.199-29G>C ENSP00000438482.1:n.199-29G>C
ENST00000542367.1:n.9G>C
ENST00000545484.1:n.281-29G>C
NM_053056.2:c.575-29G>C NP_444284.1:n.575-29G>C
XM_006718653.2:c.599-29G>C XP_006718716.1:n.599-29G>C
NM_053056.3:c.575-29G>C MANE Select NP_444284.1:n.575-29G>C
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