Canonical Allele Identifier: CA872127091

Gene: F9

Linked Data

• dbSNP Id: rs1290850016
• gnomAD v3: X-139560871-G-T
• gnomAD v4: X-139560871-G-T
• MyVariant Identifiers: chrX:g.138643030G>T (hg19) ; chrX:g.139560871G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560871G>T , CM000685.2:g.139560871G>T	GRCh38
NC_000023.10:g.138643030G>T , CM000685.1:g.138643030G>T	GRCh37
NC_000023.9:g.138470696G>T	NCBI36
NG_007994.1:g.35136G>T , LRG_556:g.35136G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.838+16G>T MANE Select	ENSP00000218099.2:n.838+16G>T
ENST00000643157.1:n.1505+16G>T
ENST00000218099.6:c.838+16G>T	ENSP00000218099.2:n.838+16G>T
ENST00000394090.2:c.724+16G>T	ENSP00000377650.2:n.724+16G>T
NM_000133.3:c.838+16G>T , LRG_556t1:c.838+16G>T	NP_000124.1:n.838+16G>T
NM_001313913.1:c.724+16G>T	NP_001300842.1:n.724+16G>T
XM_005262397.3:c.709+16G>T	XP_005262454.1:n.709+16G>T
XM_005262397.4:c.709+16G>T	XP_005262454.1:n.709+16G>T
NM_000133.4:c.838+16G>T MANE Select	NP_000124.1:n.838+16G>T
NM_001313913.2:c.724+16G>T	NP_001300842.1:n.724+16G>T