Canonical Allele Identifier: CA1097384097
Gene: FAM20C HGNC NCBI

Linked Data

dbSNP Id: rs377304861
gnomAD v3: 7-255781-G-C
gnomAD v4: 7-255781-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255781G>C , CM000669.2:g.255781G>C GRCh38
NC_000007.13:g.295747G>C , CM000669.1:g.295747G>C GRCh37
NG_033970.1:g.65417G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313766.6:c.1073-68G>C MANE Select ENSP00000322323.5:n.1073-68G>C
ENST00000313766.5:c.1073-68G>C ENSP00000322323.5:n.1073-68G>C
ENST00000515795.1:n.730-68G>C
NM_020223.3:c.1073-68G>C NP_064608.2:n.1073-68G>C
XR_242097.3:n.1220-68G>C
XM_017012450.1:c.1334-68G>C XP_016867939.1:n.1334-68G>C
XM_017012451.1:c.1331-68G>C XP_016867940.1:n.1331-68G>C
XM_017012455.2:c.371-68G>C XP_016867944.1:n.371-68G>C
NM_020223.4:c.1073-68G>C MANE Select NP_064608.2:n.1073-68G>C
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