Canonical Allele Identifier: CA366525143
Gene: FAM20C HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.295856T>A (hg19) chr7:g.255890T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255890T>A , CM000669.2:g.255890T>A GRCh38
NC_000007.13:g.295856T>A , CM000669.1:g.295856T>A GRCh37
NG_033970.1:g.65526T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313766.6:c.1114T>A MANE Select ENSP00000322323.5:p.Ser372Thr
ENST00000313766.5:c.1114T>A ENSP00000322323.5:p.Ser372Thr
ENST00000515795.1:n.771T>A
NM_020223.3:c.1114T>A NP_064608.2:p.Ser372Thr
XR_242097.3:n.1261T>A
XM_017012450.1:c.1375T>A XP_016867939.1:p.Ser459Thr
XM_017012451.1:c.1372T>A XP_016867940.1:p.Ser458Thr
XM_017012455.2:c.412T>A XP_016867944.1:p.Ser138Thr
NM_020223.4:c.1114T>A MANE Select NP_064608.2:p.Ser372Thr
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