Canonical Allele Identifier: CA255218

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860588C>A , CM000685.2:g.154860588C>A	GRCh38
NC_000023.10:g.154088863C>A , CM000685.1:g.154088863C>A	GRCh37
NC_000023.9:g.153742057C>A	NCBI36
NG_011403.1:g.167136G>T
NG_011403.2:g.167136G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000132.4:c.6744G>T MANE Select	NP_000123.1:p.Trp2248Cys
ENST00000360256.9:c.6744G>T MANE Select	ENSP00000353393.4:p.Trp2248Cys
NM_000132.3:c.6744G>T	NP_000123.1:p.Trp2248Cys
NM_019863.2:c.339G>T	NP_063916.1:p.Trp113Cys
NM_019863.3:c.339G>T	NP_063916.1:p.Trp113Cys
ENST00000330287.10:c.339G>T	ENSP00000327895.6:p.Trp113Cys
ENST00000360256.8:c.6744G>T	ENSP00000353393.4:p.Trp2248Cys
ENST00000644698.1:c.477G>T	ENSP00000495706.1:p.Trp159Cys
XM_011531126.1:c.6639G>T	XP_011529428.1:p.Trp2213Cys