Canonical Allele Identifier: CA600001864
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1206519728
gnomAD v2: 11-69464902-C-T
gnomAD v3: 11-69650134-C-T
gnomAD v4: 11-69650134-C-T
MyVariant Identifiers: chr11:g.69464902C>T (hg19) chr11:g.69650134C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69650134C>T , CM000673.2:g.69650134C>T GRCh38
NC_000011.9:g.69464902C>T , CM000673.1:g.69464902C>T GRCh37
NC_000011.8:g.69174083C>T NCBI36
NG_007375.1:g.14030C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.724-984C>T MANE Select ENSP00000227507.2:n.724-984C>T
ENST00000227507.2:c.724-984C>T ENSP00000227507.2:n.724-984C>T
ENST00000542367.1:n.187-984C>T
NM_053056.2:c.724-984C>T NP_444284.1:n.724-984C>T
XM_006718653.2:c.748-984C>T XP_006718716.1:n.748-984C>T
NM_053056.3:c.724-984C>T MANE Select NP_444284.1:n.724-984C>T
Search 100 bp 5'
Search 100 bp 3'