Canonical Allele Identifier: CA15772030
Gene: FAM124A HGNC NCBI

Linked Data

dbSNP Id: rs10492519

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51250192A>G , CM000675.2:g.51250192A>G GRCh38
NC_000013.10:g.51824328A>G , CM000675.1:g.51824328A>G GRCh37
NC_000013.9:g.50722329A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000280057.6:c.209-1276A>G ENSP00000280057.6:p.=
ENST00000322475.12:c.101-1276A>G ENSP00000324625.7:p.=
ENST00000614765.4:c.101-1276A>G ENSP00000483855.1:p.=
ENST00000615498.4:c.101-1276A>G ENSP00000481212.1:p.=
NM_001242312.1:c.101-1276A>G NP_001229241.1:p.=
NM_145019.3:c.209-1276A>G NP_659456.3:p.=
XM_011534974.1:c.89-1276A>G XP_011533276.1:p.=
XM_011534975.1:c.89-1276A>G XP_011533277.1:p.=
XM_011534976.1:c.89-1276A>G XP_011533278.1:p.=
XM_011534977.1:c.89-1276A>G XP_011533279.1:p.=
XM_011534978.1:c.209-1276A>G XP_011533280.1:p.=
XM_011534979.1:c.209-1276A>G XP_011533281.1:p.=
XM_011534980.1:c.209-1276A>G XP_011533282.1:p.=
NM_001330522.1:c.101-1276A>G NP_001317451.1:p.=
XM_011534978.2:c.209-1276A>G XP_011533280.1:p.=
XM_017020419.2:c.101-1276A>G XP_016875908.1:p.=
NM_001242312.2:c.101-1276A>G MANE Select NP_001229241.1:p.=
NM_145019.4:c.209-1276A>G NP_659456.3:p.=
NM_001330522.2:c.101-1276A>G NP_001317451.1:p.=