Canonical Allele Identifier: CA414907111

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091393G>T (hg19) ; chrX:g.154863118G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863118G>T , CM000685.2:g.154863118G>T	GRCh38
NC_000023.10:g.154091393G>T , CM000685.1:g.154091393G>T	GRCh37
NC_000023.9:g.153744587G>T	NCBI36
NG_011403.1:g.164606C>A
NG_011403.2:g.164606C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6539C>A MANE Select	ENSP00000353393.4:p.Thr2180Asn
ENST00000644698.1:c.272C>A	ENSP00000495706.1:p.Thr91Asn
ENST00000330287.10:c.134C>A	ENSP00000327895.6:p.Thr45Asn
ENST00000360256.8:c.6539C>A	ENSP00000353393.4:p.Thr2180Asn
NM_000132.3:c.6539C>A	NP_000123.1:p.Thr2180Asn
NM_019863.2:c.134C>A	NP_063916.1:p.Thr45Asn
XM_011531126.1:c.6434C>A	XP_011529428.1:p.Thr2145Asn
NM_000132.4:c.6539C>A MANE Select	NP_000123.1:p.Thr2180Asn
NM_019863.3:c.134C>A	NP_063916.1:p.Thr45Asn