Canonical Allele Identifier: CA2708219479
Gene: FBXL7 HGNC NCBI

Linked Data

dbSNP Id: rs2126723490

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.15783572A>G , CM000667.2:g.15783572A>G GRCh38
NC_000005.9:g.15783681A>G , CM000667.1:g.15783681A>G GRCh37
NC_000005.8:g.15836681A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504595.2:c.128-144318A>G MANE Select ENSP00000423630.1:n.128-144318A>G
ENST00000504595.1:c.128-144318A>G ENSP00000423630.1:n.128-144318A>G
ENST00000510662.1:c.-14-144318A>G ENSP00000425184.1:n.-14-144318A>G
NM_001278317.1:c.-14-144318A>G NP_001265246.1:n.-14-144318A>G
NM_012304.4:c.128-144318A>G NP_036436.1:n.128-144318A>G
XM_005248273.3:c.113-144318A>G XP_005248330.1:n.113-144318A>G
XM_011513998.1:c.-91-51205A>G XP_011512300.1:n.-91-51205A>G
XM_017009262.2:c.113-144318A>G XP_016864751.1:n.113-144318A>G
NM_012304.5:c.128-144318A>G MANE Select NP_036436.1:n.128-144318A>G
NM_001278317.2:c.-14-144318A>G NP_001265246.1:n.-14-144318A>G