Canonical Allele Identifier: CA414906593

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154132344C>A (hg19) ; chrX:g.154904069C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904069C>A , CM000685.2:g.154904069C>A	GRCh38
NC_000023.10:g.154132344C>A , CM000685.1:g.154132344C>A	GRCh37
NC_000023.9:g.153785538C>A	NCBI36
NG_011403.1:g.123655G>T
NG_011403.2:g.123655G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5835G>T MANE Select	ENSP00000353393.4:p.Met1945Ile
ENST00000360256.8:c.5835G>T	ENSP00000353393.4:p.Met1945Ile
NM_000132.3:c.5835G>T	NP_000123.1:p.Met1945Ile
XM_011531126.1:c.5730G>T	XP_011529428.1:p.Met1910Ile
NM_000132.4:c.5835G>T MANE Select	NP_000123.1:p.Met1945Ile