Canonical Allele Identifier: CA414897959

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154066028C>T (hg19) ; chrX:g.154837753C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837753C>T , CM000685.2:g.154837753C>T	GRCh38
NC_000023.10:g.154066028C>T , CM000685.1:g.154066028C>T	GRCh37
NC_000023.9:g.153719222C>T	NCBI36
NG_011403.1:g.189971G>A
NG_033065.1:g.1910G>A
NG_011403.2:g.189971G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6901-1G>A MANE Select	ENSP00000353393.4:n.6901-1G>A
ENST00000644698.1:c.634-1G>A	ENSP00000495706.1:n.634-1G>A
ENST00000330287.10:c.496-1G>A	ENSP00000327895.6:n.496-1G>A
ENST00000360256.8:c.6901-1G>A	ENSP00000353393.4:n.6901-1G>A
NM_000132.3:c.6901-1G>A	NP_000123.1:n.6901-1G>A
NM_019863.2:c.496-1G>A	NP_063916.1:n.496-1G>A
XM_011531126.1:c.6796-1G>A	XP_011529428.1:n.6796-1G>A
NM_000132.4:c.6901-1G>A MANE Select	NP_000123.1:n.6901-1G>A
NM_019863.3:c.496-1G>A	NP_063916.1:n.496-1G>A