Canonical Allele Identifier: CA519355736

Gene: F8

Linked Data

• gnomAD v4: X-154902058-G-A
• MyVariant Identifiers: chrX:g.154130333G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902058G>A , CM000685.2:g.154902058G>A	GRCh38
NC_000023.10:g.154130333G>A , CM000685.1:g.154130333G>A	GRCh37
NC_000023.9:g.153783527G>A	NCBI36
NG_011403.1:g.125666C>T
NG_011403.2:g.125666C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6108C>T MANE Select	ENSP00000353393.4:p.Tyr2036=
ENST00000360256.8:c.6108C>T	ENSP00000353393.4:p.Tyr2036=
NM_000132.3:c.6108C>T	NP_000123.1:p.Tyr2036=
XM_011531126.1:c.6003C>T	XP_011529428.1:p.Tyr2001=
NM_000132.4:c.6108C>T MANE Select	NP_000123.1:p.Tyr2036=