Canonical Allele Identifier: CA1681866457
Gene: FAM20C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255670G= , CM000669.2:g.255670G= GRCh38
NC_000007.13:g.295636G= , CM000669.1:g.295636G= GRCh37
NG_033970.1:g.65306G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313766.6:c.1073-179G= MANE Select ENSP00000322323.5:n.1073-179G=
ENST00000313766.5:c.1073-179G= ENSP00000322323.5:n.1073-179G=
ENST00000515795.1:n.730-179G=
NM_020223.3:c.1073-179G= NP_064608.2:n.1073-179G=
XR_242097.3:n.1220-179G=
XM_017012450.1:c.1334-179G= XP_016867939.1:n.1334-179G=
XM_017012451.1:c.1331-179G= XP_016867940.1:n.1331-179G=
XM_017012455.2:c.371-179G= XP_016867944.1:n.371-179G=
NM_020223.4:c.1073-179G= MANE Select NP_064608.2:n.1073-179G=
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