Canonical Allele Identifier: CA414907793

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091461A>T (hg19) ; chrX:g.154863186A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863186A>T , CM000685.2:g.154863186A>T	GRCh38
NC_000023.10:g.154091461A>T , CM000685.1:g.154091461A>T	GRCh37
NC_000023.9:g.153744655A>T	NCBI36
NG_011403.1:g.164538T>A
NG_011403.2:g.164538T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6471T>A MANE Select	ENSP00000353393.4:p.Asn2157Lys
ENST00000644698.1:c.204T>A	ENSP00000495706.1:p.Asn68Lys
ENST00000330287.10:c.66T>A	ENSP00000327895.6:p.Asn22Lys
ENST00000360256.8:c.6471T>A	ENSP00000353393.4:p.Asn2157Lys
NM_000132.3:c.6471T>A	NP_000123.1:p.Asn2157Lys
NM_019863.2:c.66T>A	NP_063916.1:p.Asn22Lys
XM_011531126.1:c.6366T>A	XP_011529428.1:p.Asn2122Lys
NM_000132.4:c.6471T>A MANE Select	NP_000123.1:p.Asn2157Lys
NM_019863.3:c.66T>A	NP_063916.1:p.Asn22Lys