Canonical Allele Identifier: CA414903619

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154088777T>A (hg19) ; chrX:g.154860502T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860502T>A , CM000685.2:g.154860502T>A	GRCh38
NC_000023.10:g.154088777T>A , CM000685.1:g.154088777T>A	GRCh37
NC_000023.9:g.153741971T>A	NCBI36
NG_011403.1:g.167222A>T
NG_011403.2:g.167222A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6830A>T MANE Select	ENSP00000353393.4:p.Lys2277Met
ENST00000644698.1:c.563A>T	ENSP00000495706.1:p.Lys188Met
ENST00000330287.10:c.425A>T	ENSP00000327895.6:p.Lys142Met
ENST00000360256.8:c.6830A>T	ENSP00000353393.4:p.Lys2277Met
NM_000132.3:c.6830A>T	NP_000123.1:p.Lys2277Met
NM_019863.2:c.425A>T	NP_063916.1:p.Lys142Met
XM_011531126.1:c.6725A>T	XP_011529428.1:p.Lys2242Met
NM_000132.4:c.6830A>T MANE Select	NP_000123.1:p.Lys2277Met
NM_019863.3:c.425A>T	NP_063916.1:p.Lys142Met