Canonical Allele Identifier: CA475219553
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1341859043
gnomAD v2: 11-69462850-C-T
gnomAD v4: 11-69648082-C-T
MyVariant Identifiers: chr11:g.69462850C>T (hg19) chr11:g.69648082C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648082C>T , CM000673.2:g.69648082C>T GRCh38
NC_000011.9:g.69462850C>T , CM000673.1:g.69462850C>T GRCh37
NC_000011.8:g.69172031C>T NCBI36
NG_007375.1:g.11978C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.663C>T MANE Select ENSP00000227507.2:p.Asn221=
ENST00000227507.2:c.663C>T ENSP00000227507.2:p.Asn221=
ENST00000536559.1:c.*83C>T ENSP00000438482.1:n.*83C>T
ENST00000542367.1:n.126C>T
ENST00000545484.1:n.369C>T
NM_053056.2:c.663C>T NP_444284.1:p.Asn221=
XM_006718653.2:c.687C>T XP_006718716.1:p.Asn229=
NM_053056.3:c.663C>T MANE Select NP_444284.1:p.Asn221=
Search 100 bp 5'
Search 100 bp 3'