Canonical Allele Identifier: CA414445661

Gene: F9

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561749G>A , CM000685.2:g.139561749G>A	GRCh38
NC_000023.10:g.138643908G>A , CM000685.1:g.138643908G>A	GRCh37
NC_000023.9:g.138471574G>A	NCBI36
NG_007994.1:g.36014G>A , LRG_556:g.36014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1064G>A MANE Select	ENSP00000218099.2:p.Gly355Asp
ENST00000643157.1:n.1723+8G>A
ENST00000218099.6:c.1064G>A	ENSP00000218099.2:p.Gly355Asp
ENST00000394090.2:c.950G>A	ENSP00000377650.2:p.Gly317Asp
NM_000133.3:c.1064G>A , LRG_556t1:c.1064G>A	NP_000124.1:p.Gly355Asp
NM_001313913.1:c.950G>A	NP_001300842.1:p.Gly317Asp
XM_005262397.3:c.935G>A	XP_005262454.1:p.Gly312Asp
XM_005262397.4:c.935G>A	XP_005262454.1:p.Gly312Asp
NM_000133.4:c.1064G>A MANE Select	NP_000124.1:p.Gly355Asp
NM_001313913.2:c.950G>A	NP_001300842.1:p.Gly317Asp