Canonical Allele Identifier: CA2755298
Gene: CCDC50 HGNC NCBI

Linked Data

ClinVar Variation Id: 2964551
ClinVar RCV Id: RCV003828173
dbSNP Id: rs375874806
ExAC: 3:191093045 A / G
gnomAD v2: 3-191093045-A-G
gnomAD v3: 3-191375256-A-G
gnomAD v4: 3-191375256-A-G
MyVariant Identifiers: chr3:g.191093045A>G (hg19) chr3:g.191375256A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375256A>G , CM000665.2:g.191375256A>G GRCh38
NC_000003.11:g.191093045A>G , CM000665.1:g.191093045A>G GRCh37
NC_000003.10:g.192575739A>G NCBI36
NG_008994.1:g.51172A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.643A>G MANE Select ENSP00000376249.4:p.Asn215Asp
ENST00000392456.4:c.449-4903A>G ENSP00000376250.4:n.449-4903A>G
ENST00000392455.7:c.449-4903A>G ENSP00000376249.3:n.449-4903A>G
ENST00000392456.3:c.643A>G ENSP00000376250.3:p.Asn215Asp
NM_174908.3:c.449-4903A>G NP_777568.1:n.449-4903A>G
NM_178335.2:c.643A>G NP_848018.1:p.Asn215Asp
XM_011512460.1:c.643A>G XP_011510762.1:p.Asn215Asp
NM_178335.3:c.643A>G MANE Select NP_848018.1:p.Asn215Asp
NM_174908.4:c.449-4903A>G NP_777568.1:n.449-4903A>G
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