Canonical Allele Identifier: CA2578817062
Gene: FAM20C HGNC NCBI

Linked Data

gnomAD v4: 7-255769-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255769C>T , CM000669.2:g.255769C>T GRCh38
NC_000007.13:g.295735C>T , CM000669.1:g.295735C>T GRCh37
NG_033970.1:g.65405C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313766.6:c.1073-80C>T MANE Select ENSP00000322323.5:n.1073-80C>T
ENST00000313766.5:c.1073-80C>T ENSP00000322323.5:n.1073-80C>T
ENST00000515795.1:n.730-80C>T
NM_020223.3:c.1073-80C>T NP_064608.2:n.1073-80C>T
XR_242097.3:n.1220-80C>T
XM_017012450.1:c.1334-80C>T XP_016867939.1:n.1334-80C>T
XM_017012451.1:c.1331-80C>T XP_016867940.1:n.1331-80C>T
XM_017012455.2:c.371-80C>T XP_016867944.1:n.371-80C>T
NM_020223.4:c.1073-80C>T MANE Select NP_064608.2:n.1073-80C>T
Search 100 bp 5'
Search 100 bp 3'