Canonical Allele Identifier: CA1137751073

Gene: F9

Linked Data

• dbSNP Id: rs1603267277
• gnomAD v3: X-139561298-G-T
• gnomAD v4: X-139561298-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561298G>T , CM000685.2:g.139561298G>T	GRCh38
NC_000023.10:g.138643457G>T , CM000685.1:g.138643457G>T	GRCh37
NC_000023.9:g.138471123G>T	NCBI36
NG_007994.1:g.35563G>T , LRG_556:g.35563G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.839-226G>T MANE Select	ENSP00000218099.2:n.839-226G>T
ENST00000643157.1:n.1506-226G>T
ENST00000218099.6:c.839-226G>T	ENSP00000218099.2:n.839-226G>T
ENST00000394090.2:c.725-226G>T	ENSP00000377650.2:n.725-226G>T
NM_000133.3:c.839-226G>T , LRG_556t1:c.839-226G>T	NP_000124.1:n.839-226G>T
NM_001313913.1:c.725-226G>T	NP_001300842.1:n.725-226G>T
XM_005262397.3:c.710-226G>T	XP_005262454.1:n.710-226G>T
XM_005262397.4:c.710-226G>T	XP_005262454.1:n.710-226G>T
NM_000133.4:c.839-226G>T MANE Select	NP_000124.1:n.839-226G>T
NM_001313913.2:c.725-226G>T	NP_001300842.1:n.725-226G>T