Canonical Allele Identifier: CA2695170486

Gene: F8

Linked Data

• gnomAD v4: X-155022569-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022569T>A , CM000685.2:g.155022569T>A	GRCh38
NC_000023.10:g.154250844T>A , CM000685.1:g.154250844T>A	GRCh37
NC_000023.9:g.153904038T>A	NCBI36
NG_011403.1:g.5155A>T
NG_011403.2:g.5155A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-17A>T MANE Select	ENSP00000353393.4:n.-17A>T
ENST00000647125.1:c.-17A>T	ENSP00000496062.1:n.-17A>T
ENST00000360256.8:c.-17A>T	ENSP00000353393.4:n.-17A>T
ENST00000423959.5:c.38+4211A>T	ENSP00000409446.1:n.38+4211A>T
ENST00000453950.1:c.39-73A>T	ENSP00000389153.1:n.39-73A>T
NM_000132.3:c.-17A>T	NP_000123.1:n.-17A>T
XM_011531126.1:c.38+4211A>T	XP_011529428.1:n.38+4211A>T
NM_000132.4:c.-17A>T MANE Select	NP_000123.1:n.-17A>T