Canonical Allele Identifier: CA381658008

Gene: CCND1

Linked Data

• dbSNP Id: rs2120108895
• MyVariant Identifiers: chr11:g.69462804G>T (hg19) ; chr11:g.69648036G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648036G>T , CM000673.2:g.69648036G>T	GRCh38
NC_000011.9:g.69462804G>T , CM000673.1:g.69462804G>T	GRCh37
NC_000011.8:g.69171985G>T	NCBI36
NG_007375.1:g.11932G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.617G>T MANE Select	ENSP00000227507.2:p.Gly206Val
ENST00000227507.2:c.617G>T	ENSP00000227507.2:p.Gly206Val
ENST00000536559.1:c.*37G>T	ENSP00000438482.1:n.*37G>T
ENST00000542367.1:n.80G>T
ENST00000545484.1:n.323G>T
NM_053056.2:c.617G>T	NP_444284.1:p.Gly206Val
XM_006718653.2:c.641G>T	XP_006718716.1:p.Gly214Val
NM_053056.3:c.617G>T MANE Select	NP_444284.1:p.Gly206Val