Canonical Allele Identifier: CA1590037466
Gene: FBXO38 HGNC NCBI

Linked Data

dbSNP Id: rs1384224713

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148425508T>C , CM000667.2:g.148425508T>C GRCh38
NC_000005.9:g.147805071T>C , CM000667.1:g.147805071T>C GRCh37
NC_000005.8:g.147785264T>C NCBI36
NG_033871.1:g.46574T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340253.10:c.1739-14T>C MANE Select ENSP00000342023.6:n.1739-14T>C
ENST00000296701.10:c.1739-14T>C ENSP00000296701.6:n.1739-14T>C
ENST00000340253.9:c.1739-14T>C ENSP00000342023.5:n.1739-14T>C
ENST00000394370.7:c.1739-14T>C ENSP00000377895.3:n.1739-14T>C
ENST00000513826.1:c.1739-14T>C ENSP00000426410.1:n.1739-14T>C
ENST00000514832.1:n.370-14T>C
NM_001271723.1:c.1739-14T>C NP_001258652.1:n.1739-14T>C
NM_030793.4:c.1739-14T>C NP_110420.3:n.1739-14T>C
XM_005268513.1:c.1739-14T>C XP_005268570.1:n.1739-14T>C
XM_006714797.1:c.1739-14T>C XP_006714860.1:n.1739-14T>C
XM_011537683.1:c.641-14T>C XP_011535985.1:n.641-14T>C
XM_011537684.1:c.539-14T>C XP_011535986.1:n.539-14T>C
NM_205836.2:c.1739-14T>C NP_995308.1:n.1739-14T>C
XM_006714797.2:c.1739-14T>C XP_006714860.1:n.1739-14T>C
XM_011537684.3:c.539-14T>C XP_011535986.1:n.539-14T>C
XM_017009899.1:c.641-14T>C XP_016865388.1:n.641-14T>C
XM_017009900.2:c.539-14T>C XP_016865389.1:n.539-14T>C
XM_017009901.2:c.641-14T>C XP_016865390.1:n.641-14T>C
XM_017009902.2:c.539-14T>C XP_016865391.1:n.539-14T>C
XM_024446223.1:c.1739-14T>C XP_024301991.1:n.1739-14T>C
XR_001742284.1:n.1885-14T>C
NM_030793.5:c.1739-14T>C NP_110420.3:n.1739-14T>C
NM_205836.3:c.1739-14T>C MANE Select NP_995308.1:n.1739-14T>C
NM_001271723.2:c.1739-14T>C NP_001258652.1:n.1739-14T>C