Canonical Allele Identifier: CA2695153025

Gene: F8

Linked Data

• gnomAD v4: X-154903888-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903888G>A , CM000685.2:g.154903888G>A	GRCh38
NC_000023.10:g.154132163G>A , CM000685.1:g.154132163G>A	GRCh37
NC_000023.9:g.153785357G>A	NCBI36
NG_011403.1:g.123836C>T
NG_011403.2:g.123836C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5998+18C>T MANE Select	ENSP00000353393.4:n.5998+18C>T
ENST00000360256.8:c.5998+18C>T	ENSP00000353393.4:n.5998+18C>T
NM_000132.3:c.5998+18C>T	NP_000123.1:n.5998+18C>T
XM_011531126.1:c.5893+18C>T	XP_011529428.1:n.5893+18C>T
NM_000132.4:c.5998+18C>T MANE Select	NP_000123.1:n.5998+18C>T