Canonical Allele Identifier: CA366525118
Gene: FAM20C HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.295847T>C (hg19) chr7:g.255881T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255881T>C , CM000669.2:g.255881T>C GRCh38
NC_000007.13:g.295847T>C , CM000669.1:g.295847T>C GRCh37
NG_033970.1:g.65517T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313766.6:c.1105T>C MANE Select ENSP00000322323.5:p.Tyr369His
ENST00000313766.5:c.1105T>C ENSP00000322323.5:p.Tyr369His
ENST00000515795.1:n.762T>C
NM_020223.3:c.1105T>C NP_064608.2:p.Tyr369His
XR_242097.3:n.1252T>C
XM_017012450.1:c.1366T>C XP_016867939.1:p.Tyr456His
XM_017012451.1:c.1363T>C XP_016867940.1:p.Tyr455His
XM_017012455.2:c.403T>C XP_016867944.1:p.Tyr135His
NM_020223.4:c.1105T>C MANE Select NP_064608.2:p.Tyr369His
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