Canonical Allele Identifier: CA519355190

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065902A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837627A>C , CM000685.2:g.154837627A>C	GRCh38
NC_000023.10:g.154065902A>C , CM000685.1:g.154065902A>C	GRCh37
NC_000023.9:g.153719096A>C	NCBI36
NG_011403.1:g.190097T>G
NG_033065.1:g.2036T>G
NG_011403.2:g.190097T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7026T>G MANE Select	ENSP00000353393.4:p.Val2342=
ENST00000644698.1:c.759T>G	ENSP00000495706.1:p.Val253=
ENST00000330287.10:c.621T>G	ENSP00000327895.6:p.Val207=
ENST00000360256.8:c.7026T>G	ENSP00000353393.4:p.Val2342=
NM_000132.3:c.7026T>G	NP_000123.1:p.Val2342=
NM_019863.2:c.621T>G	NP_063916.1:p.Val207=
XM_011531126.1:c.6921T>G	XP_011529428.1:p.Val2307=
NM_000132.4:c.7026T>G MANE Select	NP_000123.1:p.Val2342=
NM_019863.3:c.621T>G	NP_063916.1:p.Val207=