Canonical Allele Identifier: CA1681866566
Gene: FAM20C HGNC NCBI

Linked Data

dbSNP Id: rs1788567407
gnomAD v4: 7-255790-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255790C>T , CM000669.2:g.255790C>T GRCh38
NC_000007.13:g.295756C>T , CM000669.1:g.295756C>T GRCh37
NG_033970.1:g.65426C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313766.6:c.1073-59C>T MANE Select ENSP00000322323.5:n.1073-59C>T
ENST00000313766.5:c.1073-59C>T ENSP00000322323.5:n.1073-59C>T
ENST00000515795.1:n.730-59C>T
NM_020223.3:c.1073-59C>T NP_064608.2:n.1073-59C>T
XR_242097.3:n.1220-59C>T
XM_017012450.1:c.1334-59C>T XP_016867939.1:n.1334-59C>T
XM_017012451.1:c.1331-59C>T XP_016867940.1:n.1331-59C>T
XM_017012455.2:c.371-59C>T XP_016867944.1:n.371-59C>T
NM_020223.4:c.1073-59C>T MANE Select NP_064608.2:n.1073-59C>T
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