Canonical Allele Identifier: CA128948785
Gene: FBXO38 HGNC NCBI

Linked Data

dbSNP Id: rs900601720

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148425469T>A , CM000667.2:g.148425469T>A GRCh38
NC_000005.9:g.147805032T>A , CM000667.1:g.147805032T>A GRCh37
NC_000005.8:g.147785225T>A NCBI36
NG_033871.1:g.46535T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340253.10:c.1739-53T>A MANE Select ENSP00000342023.6:n.1739-53T>A
ENST00000296701.10:c.1739-53T>A ENSP00000296701.6:n.1739-53T>A
ENST00000340253.9:c.1739-53T>A ENSP00000342023.5:n.1739-53T>A
ENST00000394370.7:c.1739-53T>A ENSP00000377895.3:n.1739-53T>A
ENST00000513826.1:c.1739-53T>A ENSP00000426410.1:n.1739-53T>A
ENST00000514832.1:n.370-53T>A
NM_001271723.1:c.1739-53T>A NP_001258652.1:n.1739-53T>A
NM_030793.4:c.1739-53T>A NP_110420.3:n.1739-53T>A
XM_005268513.1:c.1739-53T>A XP_005268570.1:n.1739-53T>A
XM_006714797.1:c.1739-53T>A XP_006714860.1:n.1739-53T>A
XM_011537683.1:c.641-53T>A XP_011535985.1:n.641-53T>A
XM_011537684.1:c.539-53T>A XP_011535986.1:n.539-53T>A
NM_205836.2:c.1739-53T>A NP_995308.1:n.1739-53T>A
XM_006714797.2:c.1739-53T>A XP_006714860.1:n.1739-53T>A
XM_011537684.3:c.539-53T>A XP_011535986.1:n.539-53T>A
XM_017009899.1:c.641-53T>A XP_016865388.1:n.641-53T>A
XM_017009900.2:c.539-53T>A XP_016865389.1:n.539-53T>A
XM_017009901.2:c.641-53T>A XP_016865390.1:n.641-53T>A
XM_017009902.2:c.539-53T>A XP_016865391.1:n.539-53T>A
XM_024446223.1:c.1739-53T>A XP_024301991.1:n.1739-53T>A
XR_001742284.1:n.1885-53T>A
NM_030793.5:c.1739-53T>A NP_110420.3:n.1739-53T>A
NM_205836.3:c.1739-53T>A MANE Select NP_995308.1:n.1739-53T>A
NM_001271723.2:c.1739-53T>A NP_001258652.1:n.1739-53T>A