Canonical Allele Identifier: CA414896680

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065895A>T (hg19) ; chrX:g.154837620A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837620A>T , CM000685.2:g.154837620A>T	GRCh38
NC_000023.10:g.154065895A>T , CM000685.1:g.154065895A>T	GRCh37
NC_000023.9:g.153719089A>T	NCBI36
NG_011403.1:g.190104T>A
NG_033065.1:g.2043T>A
NG_011403.2:g.190104T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7033T>A MANE Select	ENSP00000353393.4:p.Cys2345Ser
ENST00000644698.1:c.766T>A	ENSP00000495706.1:p.Cys256Ser
ENST00000330287.10:c.628T>A	ENSP00000327895.6:p.Cys210Ser
ENST00000360256.8:c.7033T>A	ENSP00000353393.4:p.Cys2345Ser
NM_000132.3:c.7033T>A	NP_000123.1:p.Cys2345Ser
NM_019863.2:c.628T>A	NP_063916.1:p.Cys210Ser
XM_011531126.1:c.6928T>A	XP_011529428.1:p.Cys2310Ser
NM_000132.4:c.7033T>A MANE Select	NP_000123.1:p.Cys2345Ser
NM_019863.3:c.628T>A	NP_063916.1:p.Cys210Ser