Canonical Allele Identifier: CA2614779983
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855805500
gnomAD v4: 11-69647945-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69647945G>T , CM000673.2:g.69647945G>T GRCh38
NC_000011.9:g.69462713G>T , CM000673.1:g.69462713G>T GRCh37
NC_000011.8:g.69171894G>T NCBI36
NG_007375.1:g.11841G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.575-49G>T MANE Select ENSP00000227507.2:n.575-49G>T
ENST00000227507.2:c.575-49G>T ENSP00000227507.2:n.575-49G>T
ENST00000536559.1:c.199-49G>T ENSP00000438482.1:n.199-49G>T
ENST00000545484.1:n.281-49G>T
NM_053056.2:c.575-49G>T NP_444284.1:n.575-49G>T
XM_006718653.2:c.599-49G>T XP_006718716.1:n.599-49G>T
NM_053056.3:c.575-49G>T MANE Select NP_444284.1:n.575-49G>T
Search 100 bp 5'
Search 100 bp 3'