Canonical Allele Identifier: CA381657932
Gene: CCND1 HGNC NCBI

Linked Data

dbSNP Id: rs1282637304
gnomAD v3: 11-69648001-G-T
gnomAD v4: 11-69648001-G-T
MyVariant Identifiers: chr11:g.69462769G>T (hg19) chr11:g.69648001G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69648001G>T , CM000673.2:g.69648001G>T GRCh38
NC_000011.9:g.69462769G>T , CM000673.1:g.69462769G>T GRCh37
NC_000011.8:g.69171950G>T NCBI36
NG_007375.1:g.11897G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227507.3:c.582G>T MANE Select ENSP00000227507.2:p.Lys194Asn
ENST00000227507.2:c.582G>T ENSP00000227507.2:p.Lys194Asn
ENST00000536559.1:c.*2G>T ENSP00000438482.1:n.*2G>T
ENST00000542367.1:n.45G>T
ENST00000545484.1:n.288G>T
NM_053056.2:c.582G>T NP_444284.1:p.Lys194Asn
XM_006718653.2:c.606G>T XP_006718716.1:p.Lys202Asn
NM_053056.3:c.582G>T MANE Select NP_444284.1:p.Lys194Asn
Search 100 bp 5'
Search 100 bp 3'