Canonical Allele Identifier: CA366525132

Gene: FAM20C

Linked Data

• MyVariant Identifiers: chr7:g.295852C>G (hg19) ; chr7:g.255886C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.255886C>G , CM000669.2:g.255886C>G	GRCh38
NC_000007.13:g.295852C>G , CM000669.1:g.295852C>G	GRCh37
NG_033970.1:g.65522C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313766.6:c.1110C>G MANE Select	ENSP00000322323.5:p.Tyr370Ter
ENST00000313766.5:c.1110C>G	ENSP00000322323.5:p.Tyr370Ter
ENST00000515795.1:n.767C>G
NM_020223.3:c.1110C>G	NP_064608.2:p.Tyr370Ter
XR_242097.3:n.1257C>G
XM_017012450.1:c.1371C>G	XP_016867939.1:p.Tyr457Ter
XM_017012451.1:c.1368C>G	XP_016867940.1:p.Tyr456Ter
XM_017012455.2:c.408C>G	XP_016867944.1:p.Tyr136Ter
NM_020223.4:c.1110C>G MANE Select	NP_064608.2:p.Tyr370Ter