Canonical Allele Identifier: CA2694839529

Gene: F9

Linked Data

• gnomAD v4: X-139548245-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548245T>C , CM000685.2:g.139548245T>C	GRCh38
NC_000023.10:g.138630404T>C , CM000685.1:g.138630404T>C	GRCh37
NC_000023.9:g.138458070T>C	NCBI36
NG_007994.1:g.22510T>C , LRG_556:g.22510T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-118T>C MANE Select	ENSP00000218099.2:n.392-118T>C
ENST00000643157.1:n.1059-118T>C
ENST00000218099.6:c.392-118T>C	ENSP00000218099.2:n.392-118T>C
ENST00000394090.2:c.278-118T>C	ENSP00000377650.2:n.278-118T>C
ENST00000479617.2:n.345-118T>C
NM_000133.3:c.392-118T>C , LRG_556t1:c.392-118T>C	NP_000124.1:n.392-118T>C
NM_001313913.1:c.278-118T>C	NP_001300842.1:n.278-118T>C
XM_005262397.3:c.392-2817T>C	XP_005262454.1:n.392-2817T>C
XM_005262397.4:c.392-2817T>C	XP_005262454.1:n.392-2817T>C
NM_000133.4:c.392-118T>C MANE Select	NP_000124.1:n.392-118T>C
NM_001313913.2:c.278-118T>C	NP_001300842.1:n.278-118T>C