Canonical Allele Identifier: CA2579713848

Gene: F9

Linked Data

• gnomAD v4: X-139561455-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561455G>C , CM000685.2:g.139561455G>C	GRCh38
NC_000023.10:g.138643614G>C , CM000685.1:g.138643614G>C	GRCh37
NC_000023.9:g.138471280G>C	NCBI36
NG_007994.1:g.35720G>C , LRG_556:g.35720G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839-69G>C MANE Select	ENSP00000218099.2:n.839-69G>C
ENST00000643157.1:n.1506-69G>C
ENST00000218099.6:c.839-69G>C	ENSP00000218099.2:n.839-69G>C
ENST00000394090.2:c.725-69G>C	ENSP00000377650.2:n.725-69G>C
NM_000133.3:c.839-69G>C , LRG_556t1:c.839-69G>C	NP_000124.1:n.839-69G>C
NM_001313913.1:c.725-69G>C	NP_001300842.1:n.725-69G>C
XM_005262397.3:c.710-69G>C	XP_005262454.1:n.710-69G>C
XM_005262397.4:c.710-69G>C	XP_005262454.1:n.710-69G>C
NM_000133.4:c.839-69G>C MANE Select	NP_000124.1:n.839-69G>C
NM_001313913.2:c.725-69G>C	NP_001300842.1:n.725-69G>C