Canonical Allele Identifier: CA414437787
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139541157C>T , CM000685.2:g.139541157C>T GRCh38
NC_000023.10:g.138623316C>T , CM000685.1:g.138623316C>T GRCh37
NC_000023.9:g.138450982C>T NCBI36
NG_007994.1:g.15422C>T , LRG_556:g.15422C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.359C>T MANE Select ENSP00000218099.2:p.Pro120Leu
ENST00000218099.6:c.359C>T ENSP00000218099.2:p.Pro120Leu
ENST00000394090.2:c.277+3771C>T ENSP00000377650.2:n.277+3771C>T
ENST00000479617.2:n.312C>T
NM_000133.3:c.359C>T , LRG_556t1:c.359C>T NP_000124.1:p.Pro120Leu
NM_001313913.1:c.277+3771C>T NP_001300842.1:n.277+3771C>T
XM_005262397.3:c.359C>T XP_005262454.1:p.Pro120Leu
XM_005262397.4:c.359C>T XP_005262454.1:p.Pro120Leu
NM_000133.4:c.359C>T MANE Select NP_000124.1:p.Pro120Leu
NM_001313913.2:c.277+3771C>T NP_001300842.1:n.277+3771C>T