Canonical Allele Identifier: CA414904206

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154088816G>C (hg19) ; chrX:g.154860541G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860541G>C , CM000685.2:g.154860541G>C	GRCh38
NC_000023.10:g.154088816G>C , CM000685.1:g.154088816G>C	GRCh37
NC_000023.9:g.153742010G>C	NCBI36
NG_011403.1:g.167183C>G
NG_011403.2:g.167183C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6791C>G MANE Select	ENSP00000353393.4:p.Thr2264Ser
ENST00000644698.1:c.524C>G	ENSP00000495706.1:p.Thr175Ser
ENST00000330287.10:c.386C>G	ENSP00000327895.6:p.Thr129Ser
ENST00000360256.8:c.6791C>G	ENSP00000353393.4:p.Thr2264Ser
NM_000132.3:c.6791C>G	NP_000123.1:p.Thr2264Ser
NM_019863.2:c.386C>G	NP_063916.1:p.Thr129Ser
XM_011531126.1:c.6686C>G	XP_011529428.1:p.Thr2229Ser
NM_000132.4:c.6791C>G MANE Select	NP_000123.1:p.Thr2264Ser
NM_019863.3:c.386C>G	NP_063916.1:p.Thr129Ser