Canonical Allele Identifier: CA223474023
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs998372872
gnomAD v3: 11-69647664-C-T
gnomAD v4: 11-69647664-C-T
MyVariant Identifiers: chr11:g.69462432C>T (hg19) chr11:g.69647664C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647664C>T , CM000673.2:g.69647664C>T GRCh38
NC_000011.9:g.69462432C>T , CM000673.1:g.69462432C>T GRCh37
NC_000011.8:g.69171613C>T NCBI36
NG_007375.1:g.11560C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575-330C>T MANE Select ENSP00000227507.2:n.575-330C>T
ENST00000227507.2:c.575-330C>T ENSP00000227507.2:n.575-330C>T
ENST00000536559.1:c.199-330C>T ENSP00000438482.1:n.199-330C>T
ENST00000545484.1:n.281-330C>T
NM_053056.2:c.575-330C>T NP_444284.1:n.575-330C>T
XM_006718653.2:c.599-330C>T XP_006718716.1:n.599-330C>T
NM_053056.3:c.575-330C>T MANE Select NP_444284.1:n.575-330C>T
Search 100 bp 5'
Search 100 bp 3'