Canonical Allele Identifier: CA2695167893

Gene: F8

Linked Data

• gnomAD v4: X-154862936-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154862936G>A , CM000685.2:g.154862936G>A	GRCh38
NC_000023.10:g.154091211G>A , CM000685.1:g.154091211G>A	GRCh37
NC_000023.9:g.153744405G>A	NCBI36
NG_011403.1:g.164788C>T
NG_011403.2:g.164788C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6574+147C>T MANE Select	ENSP00000353393.4:n.6574+147C>T
ENST00000644698.1:c.307+147C>T	ENSP00000495706.1:n.307+147C>T
ENST00000330287.10:c.169+147C>T	ENSP00000327895.6:n.169+147C>T
ENST00000360256.8:c.6574+147C>T	ENSP00000353393.4:n.6574+147C>T
NM_000132.3:c.6574+147C>T	NP_000123.1:n.6574+147C>T
NM_019863.2:c.169+147C>T	NP_063916.1:n.169+147C>T
XM_011531126.1:c.6469+147C>T	XP_011529428.1:n.6469+147C>T
NM_000132.4:c.6574+147C>T MANE Select	NP_000123.1:n.6574+147C>T
NM_019863.3:c.169+147C>T	NP_063916.1:n.169+147C>T