Canonical Allele Identifier: CA414441157
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551226G>A , CM000685.2:g.139551226G>A GRCh38
NC_000023.10:g.138633385G>A , CM000685.1:g.138633385G>A GRCh37
NC_000023.9:g.138461051G>A NCBI36
NG_007994.1:g.25491G>A , LRG_556:g.25491G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.685G>A MANE Select ENSP00000218099.2:p.Gly229Ser
ENST00000643157.1:n.1352G>A
ENST00000218099.6:c.685G>A ENSP00000218099.2:p.Gly229Ser
ENST00000394090.2:c.571G>A ENSP00000377650.2:p.Gly191Ser
NM_000133.3:c.685G>A , LRG_556t1:c.685G>A NP_000124.1:p.Gly229Ser
NM_001313913.1:c.571G>A NP_001300842.1:p.Gly191Ser
XM_005262397.3:c.556G>A XP_005262454.1:p.Gly186Ser
XM_005262397.4:c.556G>A XP_005262454.1:p.Gly186Ser
NM_000133.4:c.685G>A MANE Select NP_000124.1:p.Gly229Ser
NM_001313913.2:c.571G>A NP_001300842.1:p.Gly191Ser