Canonical Allele Identifier: CA2614780068
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1855810569
gnomAD v4: 11-69648255-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648255G>T , CM000673.2:g.69648255G>T GRCh38
NC_000011.9:g.69463023G>T , CM000673.1:g.69463023G>T GRCh37
NC_000011.8:g.69172204G>T NCBI36
NG_007375.1:g.12151G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+113G>T MANE Select ENSP00000227507.2:n.723+113G>T
ENST00000227507.2:c.723+113G>T ENSP00000227507.2:n.723+113G>T
ENST00000542367.1:n.186+113G>T
NM_053056.2:c.723+113G>T NP_444284.1:n.723+113G>T
XM_006718653.2:c.747+113G>T XP_006718716.1:n.747+113G>T
NM_053056.3:c.723+113G>T MANE Select NP_444284.1:n.723+113G>T
Search 100 bp 5'
Search 100 bp 3'