Canonical Allele Identifier: CA2614780001
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1389923822
gnomAD v4: 11-69648151-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648151G>C , CM000673.2:g.69648151G>C GRCh38
NC_000011.9:g.69462919G>C , CM000673.1:g.69462919G>C GRCh37
NC_000011.8:g.69172100G>C NCBI36
NG_007375.1:g.12047G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227507.3:c.723+9G>C MANE Select ENSP00000227507.2:n.723+9G>C
ENST00000227507.2:c.723+9G>C ENSP00000227507.2:n.723+9G>C
ENST00000536559.1:c.*152G>C ENSP00000438482.1:n.*152G>C
ENST00000542367.1:n.186+9G>C
NM_053056.2:c.723+9G>C NP_444284.1:n.723+9G>C
XM_006718653.2:c.747+9G>C XP_006718716.1:n.747+9G>C
NM_053056.3:c.723+9G>C MANE Select NP_444284.1:n.723+9G>C
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