Canonical Allele Identifier: CA1681866560
Gene: FAM20C HGNC NCBI

Linked Data

dbSNP Id: rs1441055517
gnomAD v4: 7-255782-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.255782C>A , CM000669.2:g.255782C>A GRCh38
NC_000007.13:g.295748C>A , CM000669.1:g.295748C>A GRCh37
NG_033970.1:g.65418C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000313766.6:c.1073-67C>A MANE Select ENSP00000322323.5:n.1073-67C>A
ENST00000313766.5:c.1073-67C>A ENSP00000322323.5:n.1073-67C>A
ENST00000515795.1:n.730-67C>A
NM_020223.3:c.1073-67C>A NP_064608.2:n.1073-67C>A
XR_242097.3:n.1220-67C>A
XM_017012450.1:c.1334-67C>A XP_016867939.1:n.1334-67C>A
XM_017012451.1:c.1331-67C>A XP_016867940.1:n.1331-67C>A
XM_017012455.2:c.371-67C>A XP_016867944.1:n.371-67C>A
NM_020223.4:c.1073-67C>A MANE Select NP_064608.2:n.1073-67C>A
Search 100 bp 5'
Search 100 bp 3'