Canonical Allele Identifier: CA223474700

Gene: CCND1

Linked Data

• dbSNP Id: rs902802109
• gnomAD v4: 11-69648233-C-T
• MyVariant Identifiers: chr11:g.69463001C>T (hg19) ; chr11:g.69648233C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69648233C>T , CM000673.2:g.69648233C>T	GRCh38
NC_000011.9:g.69463001C>T , CM000673.1:g.69463001C>T	GRCh37
NC_000011.8:g.69172182C>T	NCBI36
NG_007375.1:g.12129C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227507.3:c.723+91C>T MANE Select	ENSP00000227507.2:n.723+91C>T
ENST00000227507.2:c.723+91C>T	ENSP00000227507.2:n.723+91C>T
ENST00000536559.1:c.*234C>T	ENSP00000438482.1:n.*234C>T
ENST00000542367.1:n.186+91C>T
NM_053056.2:c.723+91C>T	NP_444284.1:n.723+91C>T
XM_006718653.2:c.747+91C>T	XP_006718716.1:n.747+91C>T
NM_053056.3:c.723+91C>T MANE Select	NP_444284.1:n.723+91C>T