Canonical Allele Identifier: CA15825503
Gene: FAM179B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1053667

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073835T>C , CM000676.2:g.45073835T>C GRCh38
NC_000014.8:g.45543038T>C , CM000676.1:g.45543038T>C GRCh37
NC_000014.7:g.44612788T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001308120.1:c.*274T>C VV NP_001295049.1:p.=
NM_015091.2:c.*274T>C VV
NM_015091.3:c.*274T>C VV NP_055906.2:p.=
NR_131765.1:n.5659T>C
XM_011536571.1:c.*579T>C XP_011534873.1:p.=
XM_017021098.1:c.*274T>C XP_016876587.1:p.=
XM_017021099.1:c.*274T>C XP_016876588.1:p.=
XR_001750194.1:n.5923T>C
XR_001750195.1:n.5566T>C
NM_001308120.2:c.*274T>C VV MANE Preferred
ENST00000361462.6:c.*274T>C ENSP00000354917.2:p.=
ENST00000361577.7:c.*274T>C ENSP00000355045.3:p.=
ENST00000557423.5:c.*2439T>C ENSP00000451829.1:p.=