Canonical Allele Identifier: CA414920009

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154225312C>A (hg19) ; chrX:g.154997037C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997037C>A , CM000685.2:g.154997037C>A	GRCh38
NC_000023.10:g.154225312C>A , CM000685.1:g.154225312C>A	GRCh37
NC_000023.9:g.153878506C>A	NCBI36
NG_011403.1:g.30687G>T
NG_011403.2:g.30687G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.324G>T MANE Select	ENSP00000353393.4:p.Lys108Asn
ENST00000647125.1:c.*110G>T	ENSP00000496062.1:n.*110G>T
ENST00000360256.8:c.324G>T	ENSP00000353393.4:p.Lys108Asn
ENST00000423959.5:c.219G>T	ENSP00000409446.1:p.Lys73Asn
ENST00000453950.1:c.306G>T	ENSP00000389153.1:p.Lys102Asn
NM_000132.3:c.324G>T	NP_000123.1:p.Lys108Asn
XM_011531126.1:c.219G>T	XP_011529428.1:p.Lys73Asn
NM_000132.4:c.324G>T MANE Select	NP_000123.1:p.Lys108Asn