Canonical Allele Identifier: CA414897810

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154066014T>A (hg19) ; chrX:g.154837739T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837739T>A , CM000685.2:g.154837739T>A	GRCh38
NC_000023.10:g.154066014T>A , CM000685.1:g.154066014T>A	GRCh37
NC_000023.9:g.153719208T>A	NCBI36
NG_011403.1:g.189985A>T
NG_033065.1:g.1924A>T
NG_011403.2:g.189985A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6914A>T MANE Select	ENSP00000353393.4:p.Asn2305Ile
ENST00000644698.1:c.647A>T	ENSP00000495706.1:p.Asn216Ile
ENST00000330287.10:c.509A>T	ENSP00000327895.6:p.Asn170Ile
ENST00000360256.8:c.6914A>T	ENSP00000353393.4:p.Asn2305Ile
NM_000132.3:c.6914A>T	NP_000123.1:p.Asn2305Ile
NM_019863.2:c.509A>T	NP_063916.1:p.Asn170Ile
XM_011531126.1:c.6809A>T	XP_011529428.1:p.Asn2270Ile
NM_000132.4:c.6914A>T MANE Select	NP_000123.1:p.Asn2305Ile
NM_019863.3:c.509A>T	NP_063916.1:p.Asn170Ile