Canonical Allele Identifier: CA2724289736
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855802654
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647799G>A , CM000673.2:g.69647799G>A GRCh38
NC_000011.9:g.69462567G>A , CM000673.1:g.69462567G>A GRCh37
NC_000011.8:g.69171748G>A NCBI36
NG_007375.1:g.11695G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575-195G>A MANE Select ENSP00000227507.2:n.575-195G>A
ENST00000227507.2:c.575-195G>A ENSP00000227507.2:n.575-195G>A
ENST00000536559.1:c.199-195G>A ENSP00000438482.1:n.199-195G>A
ENST00000545484.1:n.281-195G>A
NM_053056.2:c.575-195G>A NP_444284.1:n.575-195G>A
XM_006718653.2:c.599-195G>A XP_006718716.1:n.599-195G>A
NM_053056.3:c.575-195G>A MANE Select NP_444284.1:n.575-195G>A
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