Canonical Allele Identifier: CA2695167697

Gene: F8

Linked Data

• gnomAD v4: X-154860349-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860349T>A , CM000685.2:g.154860349T>A	GRCh38
NC_000023.10:g.154088624T>A , CM000685.1:g.154088624T>A	GRCh37
NC_000023.9:g.153741818T>A	NCBI36
NG_011403.1:g.167375A>T
NG_011403.2:g.167375A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+83A>T MANE Select	ENSP00000353393.4:n.6900+83A>T
ENST00000644698.1:c.633+83A>T	ENSP00000495706.1:n.633+83A>T
ENST00000330287.10:c.495+83A>T	ENSP00000327895.6:n.495+83A>T
ENST00000360256.8:c.6900+83A>T	ENSP00000353393.4:n.6900+83A>T
NM_000132.3:c.6900+83A>T	NP_000123.1:n.6900+83A>T
NM_019863.2:c.495+83A>T	NP_063916.1:n.495+83A>T
XM_011531126.1:c.6795+83A>T	XP_011529428.1:n.6795+83A>T
NM_000132.4:c.6900+83A>T MANE Select	NP_000123.1:n.6900+83A>T
NM_019863.3:c.495+83A>T	NP_063916.1:n.495+83A>T