Canonical Allele Identifier: CA414907884

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091477G>A (hg19) ; chrX:g.154863202G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863202G>A , CM000685.2:g.154863202G>A	GRCh38
NC_000023.10:g.154091477G>A , CM000685.1:g.154091477G>A	GRCh37
NC_000023.9:g.153744671G>A	NCBI36
NG_011403.1:g.164522C>T
NG_011403.2:g.164522C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6455C>T MANE Select	ENSP00000353393.4:p.Ser2152Phe
ENST00000644698.1:c.188C>T	ENSP00000495706.1:p.Ser63Phe
ENST00000330287.10:c.50C>T	ENSP00000327895.6:p.Ser17Phe
ENST00000360256.8:c.6455C>T	ENSP00000353393.4:p.Ser2152Phe
NM_000132.3:c.6455C>T	NP_000123.1:p.Ser2152Phe
NM_019863.2:c.50C>T	NP_063916.1:p.Ser17Phe
XM_011531126.1:c.6350C>T	XP_011529428.1:p.Ser2117Phe
NM_000132.4:c.6455C>T MANE Select	NP_000123.1:p.Ser2152Phe
NM_019863.3:c.50C>T	NP_063916.1:p.Ser17Phe