Canonical Allele Identifier: CA1681866555
Gene: FAM20C HGNC NCBI

Linked Data

dbSNP Id: rs1788566076
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255780G>C , CM000669.2:g.255780G>C GRCh38
NC_000007.13:g.295746G>C , CM000669.1:g.295746G>C GRCh37
NG_033970.1:g.65416G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000313766.6:c.1073-69G>C MANE Select ENSP00000322323.5:n.1073-69G>C
ENST00000313766.5:c.1073-69G>C ENSP00000322323.5:n.1073-69G>C
ENST00000515795.1:n.730-69G>C
NM_020223.3:c.1073-69G>C NP_064608.2:n.1073-69G>C
XR_242097.3:n.1220-69G>C
XM_017012450.1:c.1334-69G>C XP_016867939.1:n.1334-69G>C
XM_017012451.1:c.1331-69G>C XP_016867940.1:n.1331-69G>C
XM_017012455.2:c.371-69G>C XP_016867944.1:n.371-69G>C
NM_020223.4:c.1073-69G>C MANE Select NP_064608.2:n.1073-69G>C
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