Canonical Allele Identifier: CA2614779952
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120107856
gnomAD v4: 11-69647905-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647905C>A , CM000673.2:g.69647905C>A GRCh38
NC_000011.9:g.69462673C>A , CM000673.1:g.69462673C>A GRCh37
NC_000011.8:g.69171854C>A NCBI36
NG_007375.1:g.11801C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575-89C>A MANE Select ENSP00000227507.2:n.575-89C>A
ENST00000227507.2:c.575-89C>A ENSP00000227507.2:n.575-89C>A
ENST00000536559.1:c.199-89C>A ENSP00000438482.1:n.199-89C>A
ENST00000545484.1:n.281-89C>A
NM_053056.2:c.575-89C>A NP_444284.1:n.575-89C>A
XM_006718653.2:c.599-89C>A XP_006718716.1:n.599-89C>A
NM_053056.3:c.575-89C>A MANE Select NP_444284.1:n.575-89C>A
Search 100 bp 5'
Search 100 bp 3'