Canonical Allele Identifier: CA3497380
Gene: FBXO38 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10043775

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148425557T>C , CM000667.2:g.148425557T>C GRCh38
NC_000005.9:g.147805120T>C , CM000667.1:g.147805120T>C GRCh37
NC_000005.8:g.147785313T>C NCBI36
NG_033871.1:g.46623T>C

Transcript Alleles

HGVS Amino-acid change
NM_001271723.1:c.1774T>C VV NP_001258652.1:p.Ser592Pro
NM_030793.4:c.1774T>C VV NP_110420.3:p.Ser592Pro
XM_005268513.1:c.1774T>C XP_005268570.1:p.Ser592Pro
XM_006714797.1:c.1774T>C XP_006714860.1:p.Ser592Pro
XM_011537683.1:c.676T>C XP_011535985.1:p.Ser226Pro
XM_011537684.1:c.574T>C XP_011535986.1:p.Ser192Pro
NM_205836.2:c.1774T>C VV NP_995308.1:p.Ser592Pro
XM_006714797.2:c.1774T>C
XM_011537684.3:c.574T>C
XM_017009899.1:c.676T>C XP_016865388.1:p.Ser226Pro
XM_017009900.2:c.574T>C XP_016865389.1:p.Ser192Pro
XM_017009901.2:c.676T>C XP_016865390.1:p.Ser226Pro
XM_017009902.2:c.574T>C XP_016865391.1:p.Ser192Pro
XM_024446223.1:c.1774T>C XP_024301991.1:p.Ser592Pro
XR_001742284.1:n.1920T>C
ENST00000296701.10:c.1774T>C ENSP00000296701.6:p.Ser592Pro
ENST00000340253.9:c.1774T>C ENSP00000342023.5:p.Ser592Pro
ENST00000394370.7:c.1774T>C ENSP00000377895.3:p.Ser592Pro
ENST00000513826.1:c.1774T>C ENSP00000426410.1:p.Ser592Pro
ENST00000514832.1:n.405T>C