Canonical Allele Identifier: CA381657980
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs2120108784
MyVariant Identifiers: chr11:g.69462791A>G (hg19) chr11:g.69648023A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648023A>G , CM000673.2:g.69648023A>G GRCh38
NC_000011.9:g.69462791A>G , CM000673.1:g.69462791A>G GRCh37
NC_000011.8:g.69171972A>G NCBI36
NG_007375.1:g.11919A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.604A>G MANE Select ENSP00000227507.2:p.Met202Val
ENST00000227507.2:c.604A>G ENSP00000227507.2:p.Met202Val
ENST00000536559.1:c.*24A>G ENSP00000438482.1:n.*24A>G
ENST00000542367.1:n.67A>G
ENST00000545484.1:n.310A>G
NM_053056.2:c.604A>G NP_444284.1:p.Met202Val
XM_006718653.2:c.628A>G XP_006718716.1:p.Met210Val
NM_053056.3:c.604A>G MANE Select NP_444284.1:p.Met202Val
Search 100 bp 5'
Search 100 bp 3'