Canonical Allele Identifier: CA519352393

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154124367G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896092G>C , CM000685.2:g.154896092G>C	GRCh38
NC_000023.10:g.154124367G>C , CM000685.1:g.154124367G>C	GRCh37
NC_000023.9:g.153777561G>C	NCBI36
NG_011403.1:g.131632C>G
NG_011403.2:g.131632C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6414C>G MANE Select	ENSP00000353393.4:p.Ser2138=
ENST00000360256.8:c.6414C>G	ENSP00000353393.4:p.Ser2138=
NM_000132.3:c.6414C>G	NP_000123.1:p.Ser2138=
XM_011531126.1:c.6309C>G	XP_011529428.1:p.Ser2103=
NM_000132.4:c.6414C>G MANE Select	NP_000123.1:p.Ser2138=