Canonical Allele Identifier: CA366525126
Gene: FAM20C HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.295850T>C (hg19) chr7:g.255884T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255884T>C , CM000669.2:g.255884T>C GRCh38
NC_000007.13:g.295850T>C , CM000669.1:g.295850T>C GRCh37
NG_033970.1:g.65520T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313766.6:c.1108T>C MANE Select ENSP00000322323.5:p.Tyr370His
ENST00000313766.5:c.1108T>C ENSP00000322323.5:p.Tyr370His
ENST00000515795.1:n.765T>C
NM_020223.3:c.1108T>C NP_064608.2:p.Tyr370His
XR_242097.3:n.1255T>C
XM_017012450.1:c.1369T>C XP_016867939.1:p.Tyr457His
XM_017012451.1:c.1366T>C XP_016867940.1:p.Tyr456His
XM_017012455.2:c.406T>C XP_016867944.1:p.Tyr136His
NM_020223.4:c.1108T>C MANE Select NP_064608.2:p.Tyr370His
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