Canonical Allele Identifier: CA414906903

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091369C>G (hg19) ; chrX:g.154863094C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863094C>G , CM000685.2:g.154863094C>G	GRCh38
NC_000023.10:g.154091369C>G , CM000685.1:g.154091369C>G	GRCh37
NC_000023.9:g.153744563C>G	NCBI36
NG_011403.1:g.164630G>C
NG_011403.2:g.164630G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6563G>C MANE Select	ENSP00000353393.4:p.Cys2188Ser
ENST00000644698.1:c.296G>C	ENSP00000495706.1:p.Cys99Ser
ENST00000330287.10:c.158G>C	ENSP00000327895.6:p.Cys53Ser
ENST00000360256.8:c.6563G>C	ENSP00000353393.4:p.Cys2188Ser
NM_000132.3:c.6563G>C	NP_000123.1:p.Cys2188Ser
NM_019863.2:c.158G>C	NP_063916.1:p.Cys53Ser
XM_011531126.1:c.6458G>C	XP_011529428.1:p.Cys2153Ser
NM_000132.4:c.6563G>C MANE Select	NP_000123.1:p.Cys2188Ser
NM_019863.3:c.158G>C	NP_063916.1:p.Cys53Ser