Canonical Allele Identifier: CA679683119
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1482649057
gnomAD v3: 11-69648348-C-T
gnomAD v4: 11-69648348-C-T
MyVariant Identifiers: chr11:g.69463116C>T (hg19) chr11:g.69648348C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648348C>T , CM000673.2:g.69648348C>T GRCh38
NC_000011.9:g.69463116C>T , CM000673.1:g.69463116C>T GRCh37
NC_000011.8:g.69172297C>T NCBI36
NG_007375.1:g.12244C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.723+206C>T MANE Select ENSP00000227507.2:n.723+206C>T
ENST00000227507.2:c.723+206C>T ENSP00000227507.2:n.723+206C>T
ENST00000542367.1:n.186+206C>T
NM_053056.2:c.723+206C>T NP_444284.1:n.723+206C>T
XM_006718653.2:c.747+206C>T XP_006718716.1:n.747+206C>T
NM_053056.3:c.723+206C>T MANE Select NP_444284.1:n.723+206C>T
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