Canonical Allele Identifier: CA519355282

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065974T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837699T>C , CM000685.2:g.154837699T>C	GRCh38
NC_000023.10:g.154065974T>C , CM000685.1:g.154065974T>C	GRCh37
NC_000023.9:g.153719168T>C	NCBI36
NG_011403.1:g.190025A>G
NG_033065.1:g.1964A>G
NG_011403.2:g.190025A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6954A>G MANE Select	ENSP00000353393.4:p.Pro2318=
ENST00000644698.1:c.687A>G	ENSP00000495706.1:p.Pro229=
ENST00000330287.10:c.549A>G	ENSP00000327895.6:p.Pro183=
ENST00000360256.8:c.6954A>G	ENSP00000353393.4:p.Pro2318=
NM_000132.3:c.6954A>G	NP_000123.1:p.Pro2318=
NM_019863.2:c.549A>G	NP_063916.1:p.Pro183=
XM_011531126.1:c.6849A>G	XP_011529428.1:p.Pro2283=
NM_000132.4:c.6954A>G MANE Select	NP_000123.1:p.Pro2318=
NM_019863.3:c.549A>G	NP_063916.1:p.Pro183=