Canonical Allele Identifier: CA1137751127

Gene: F9

Linked Data

• dbSNP Id: rs1928099262
• gnomAD v3: X-139561435-A-C
• gnomAD v4: X-139561435-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561435A>C , CM000685.2:g.139561435A>C	GRCh38
NC_000023.10:g.138643594A>C , CM000685.1:g.138643594A>C	GRCh37
NC_000023.9:g.138471260A>C	NCBI36
NG_007994.1:g.35700A>C , LRG_556:g.35700A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839-89A>C MANE Select	ENSP00000218099.2:n.839-89A>C
ENST00000643157.1:n.1506-89A>C
ENST00000218099.6:c.839-89A>C	ENSP00000218099.2:n.839-89A>C
ENST00000394090.2:c.725-89A>C	ENSP00000377650.2:n.725-89A>C
NM_000133.3:c.839-89A>C , LRG_556t1:c.839-89A>C	NP_000124.1:n.839-89A>C
NM_001313913.1:c.725-89A>C	NP_001300842.1:n.725-89A>C
XM_005262397.3:c.710-89A>C	XP_005262454.1:n.710-89A>C
XM_005262397.4:c.710-89A>C	XP_005262454.1:n.710-89A>C
NM_000133.4:c.839-89A>C MANE Select	NP_000124.1:n.839-89A>C
NM_001313913.2:c.725-89A>C	NP_001300842.1:n.725-89A>C