Canonical Allele Identifier: CA519357800

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091371G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863096G>C , CM000685.2:g.154863096G>C	GRCh38
NC_000023.10:g.154091371G>C , CM000685.1:g.154091371G>C	GRCh37
NC_000023.9:g.153744565G>C	NCBI36
NG_011403.1:g.164628C>G
NG_011403.2:g.164628C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6561C>G MANE Select	ENSP00000353393.4:p.Gly2187=
ENST00000644698.1:c.294C>G	ENSP00000495706.1:p.Gly98=
ENST00000330287.10:c.156C>G	ENSP00000327895.6:p.Gly52=
ENST00000360256.8:c.6561C>G	ENSP00000353393.4:p.Gly2187=
NM_000132.3:c.6561C>G	NP_000123.1:p.Gly2187=
NM_019863.2:c.156C>G	NP_063916.1:p.Gly52=
XM_011531126.1:c.6456C>G	XP_011529428.1:p.Gly2152=
NM_000132.4:c.6561C>G MANE Select	NP_000123.1:p.Gly2187=
NM_019863.3:c.156C>G	NP_063916.1:p.Gly52=