Canonical Allele Identifier: CA1681866541
Gene: FAM20C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255771G= , CM000669.2:g.255771G= GRCh38
NC_000007.13:g.295737G= , CM000669.1:g.295737G= GRCh37
NG_033970.1:g.65407G=

Transcript Alleles

HGVS Amino-acid change
ENST00000313766.6:c.1073-78G= MANE Select ENSP00000322323.5:n.1073-78G=
ENST00000313766.5:c.1073-78G= ENSP00000322323.5:n.1073-78G=
ENST00000515795.1:n.730-78G=
NM_020223.3:c.1073-78G= NP_064608.2:n.1073-78G=
XR_242097.3:n.1220-78G=
XM_017012450.1:c.1334-78G= XP_016867939.1:n.1334-78G=
XM_017012451.1:c.1331-78G= XP_016867940.1:n.1331-78G=
XM_017012455.2:c.371-78G= XP_016867944.1:n.371-78G=
NM_020223.4:c.1073-78G= MANE Select NP_064608.2:n.1073-78G=
Search 100 bp 5'
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