Canonical Allele Identifier: CA223474133
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs900676385
gnomAD v2: 11-69462575-C-T
gnomAD v3: 11-69647807-C-T
gnomAD v4: 11-69647807-C-T
MyVariant Identifiers: chr11:g.69462575C>T (hg19) chr11:g.69647807C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647807C>T , CM000673.2:g.69647807C>T GRCh38
NC_000011.9:g.69462575C>T , CM000673.1:g.69462575C>T GRCh37
NC_000011.8:g.69171756C>T NCBI36
NG_007375.1:g.11703C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575-187C>T MANE Select ENSP00000227507.2:n.575-187C>T
ENST00000227507.2:c.575-187C>T ENSP00000227507.2:n.575-187C>T
ENST00000536559.1:c.199-187C>T ENSP00000438482.1:n.199-187C>T
ENST00000545484.1:n.281-187C>T
NM_053056.2:c.575-187C>T NP_444284.1:n.575-187C>T
XM_006718653.2:c.599-187C>T XP_006718716.1:n.599-187C>T
NM_053056.3:c.575-187C>T MANE Select NP_444284.1:n.575-187C>T
Search 100 bp 5'
Search 100 bp 3'