Canonical Allele Identifier: CA366525050
Gene: FAM20C HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.295819C>A (hg19) chr7:g.255853C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255853C>A , CM000669.2:g.255853C>A GRCh38
NC_000007.13:g.295819C>A , CM000669.1:g.295819C>A GRCh37
NG_033970.1:g.65489C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313766.6:c.1077C>A MANE Select ENSP00000322323.5:p.Asn359Lys
ENST00000313766.5:c.1077C>A ENSP00000322323.5:p.Asn359Lys
ENST00000515795.1:n.734C>A
NM_020223.3:c.1077C>A NP_064608.2:p.Asn359Lys
XR_242097.3:n.1224C>A
XM_017012450.1:c.1338C>A XP_016867939.1:p.Asn446Lys
XM_017012451.1:c.1335C>A XP_016867940.1:p.Asn445Lys
XM_017012455.2:c.375C>A XP_016867944.1:p.Asn125Lys
NM_020223.4:c.1077C>A MANE Select NP_064608.2:p.Asn359Lys
Search 100 bp 5'
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