Canonical Allele Identifier: CA414906796

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091360T>A (hg19) ; chrX:g.154863085T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863085T>A , CM000685.2:g.154863085T>A	GRCh38
NC_000023.10:g.154091360T>A , CM000685.1:g.154091360T>A	GRCh37
NC_000023.9:g.153744554T>A	NCBI36
NG_011403.1:g.164639A>T
NG_011403.2:g.164639A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6572A>T MANE Select	ENSP00000353393.4:p.Asn2191Ile
ENST00000644698.1:c.305A>T	ENSP00000495706.1:p.Asn102Ile
ENST00000330287.10:c.167A>T	ENSP00000327895.6:p.Asn56Ile
ENST00000360256.8:c.6572A>T	ENSP00000353393.4:p.Asn2191Ile
NM_000132.3:c.6572A>T	NP_000123.1:p.Asn2191Ile
NM_019863.2:c.167A>T	NP_063916.1:p.Asn56Ile
XM_011531126.1:c.6467A>T	XP_011529428.1:p.Asn2156Ile
NM_000132.4:c.6572A>T MANE Select	NP_000123.1:p.Asn2191Ile
NM_019863.3:c.167A>T	NP_063916.1:p.Asn56Ile