Canonical Allele Identifier: CA381658202

Gene: CCND1

Linked Data

• dbSNP Id: rs2120110120
• gnomAD v4: 11-69648129-T-C
• MyVariant Identifiers: chr11:g.69462897T>C (hg19) ; chr11:g.69648129T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648129T>C , CM000673.2:g.69648129T>C	GRCh38
NC_000011.9:g.69462897T>C , CM000673.1:g.69462897T>C	GRCh37
NC_000011.8:g.69172078T>C	NCBI36
NG_007375.1:g.12025T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.710T>C MANE Select	ENSP00000227507.2:p.Ile237Thr
ENST00000227507.2:c.710T>C	ENSP00000227507.2:p.Ile237Thr
ENST00000536559.1:c.*130T>C	ENSP00000438482.1:n.*130T>C
ENST00000542367.1:n.173T>C
ENST00000545484.1:n.416T>C
NM_053056.2:c.710T>C	NP_444284.1:p.Ile237Thr
XM_006718653.2:c.734T>C	XP_006718716.1:p.Ile245Thr
NM_053056.3:c.710T>C MANE Select	NP_444284.1:p.Ile237Thr