Canonical Allele Identifier: CA2578817064
Gene: FAM20C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255773C>A , CM000669.2:g.255773C>A GRCh38
NC_000007.13:g.295739C>A , CM000669.1:g.295739C>A GRCh37
NG_033970.1:g.65409C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000313766.6:c.1073-76C>A MANE Select ENSP00000322323.5:n.1073-76C>A
ENST00000313766.5:c.1073-76C>A ENSP00000322323.5:n.1073-76C>A
ENST00000515795.1:n.730-76C>A
NM_020223.3:c.1073-76C>A NP_064608.2:n.1073-76C>A
XR_242097.3:n.1220-76C>A
XM_017012450.1:c.1334-76C>A XP_016867939.1:n.1334-76C>A
XM_017012451.1:c.1331-76C>A XP_016867940.1:n.1331-76C>A
XM_017012455.2:c.371-76C>A XP_016867944.1:n.371-76C>A
NM_020223.4:c.1073-76C>A MANE Select NP_064608.2:n.1073-76C>A
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