Canonical Allele Identifier: CA519355281

Gene: F8

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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