Canonical Allele Identifier: CA2708219680
Gene: FBXL7 HGNC NCBI

Linked Data

dbSNP Id: rs2126723851

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.15783881T>G , CM000667.2:g.15783881T>G GRCh38
NC_000005.9:g.15783990T>G , CM000667.1:g.15783990T>G GRCh37
NC_000005.8:g.15836990T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504595.2:c.128-144009T>G MANE Select ENSP00000423630.1:n.128-144009T>G
ENST00000504595.1:c.128-144009T>G ENSP00000423630.1:n.128-144009T>G
ENST00000510662.1:c.-14-144009T>G ENSP00000425184.1:n.-14-144009T>G
NM_001278317.1:c.-14-144009T>G NP_001265246.1:n.-14-144009T>G
NM_012304.4:c.128-144009T>G NP_036436.1:n.128-144009T>G
XM_005248273.3:c.113-144009T>G XP_005248330.1:n.113-144009T>G
XM_011513998.1:c.-91-50896T>G XP_011512300.1:n.-91-50896T>G
XM_017009262.2:c.113-144009T>G XP_016864751.1:n.113-144009T>G
NM_012304.5:c.128-144009T>G MANE Select NP_036436.1:n.128-144009T>G
NM_001278317.2:c.-14-144009T>G NP_001265246.1:n.-14-144009T>G