Canonical Allele Identifier: CA223476394
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs542237883
gnomAD v3: 11-69649974-A-T
gnomAD v4: 11-69649974-A-T
MyVariant Identifiers: chr11:g.69464742A>T (hg19) chr11:g.69649974A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69649974A>T , CM000673.2:g.69649974A>T GRCh38
NC_000011.9:g.69464742A>T , CM000673.1:g.69464742A>T GRCh37
NC_000011.8:g.69173923A>T NCBI36
NG_007375.1:g.13870A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.724-1144A>T MANE Select ENSP00000227507.2:n.724-1144A>T
ENST00000227507.2:c.724-1144A>T ENSP00000227507.2:n.724-1144A>T
ENST00000542367.1:n.187-1144A>T
NM_053056.2:c.724-1144A>T NP_444284.1:n.724-1144A>T
XM_006718653.2:c.748-1144A>T XP_006718716.1:n.748-1144A>T
NM_053056.3:c.724-1144A>T MANE Select NP_444284.1:n.724-1144A>T
Search 100 bp 5'
Search 100 bp 3'