Canonical Allele Identifier: CA2695167949

Gene: F8

Linked Data

• gnomAD v4: X-154863064-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863064G>T , CM000685.2:g.154863064G>T	GRCh38
NC_000023.10:g.154091339G>T , CM000685.1:g.154091339G>T	GRCh37
NC_000023.9:g.153744533G>T	NCBI36
NG_011403.1:g.164660C>A
NG_011403.2:g.164660C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6574+19C>A MANE Select	ENSP00000353393.4:n.6574+19C>A
ENST00000644698.1:c.307+19C>A	ENSP00000495706.1:n.307+19C>A
ENST00000330287.10:c.169+19C>A	ENSP00000327895.6:n.169+19C>A
ENST00000360256.8:c.6574+19C>A	ENSP00000353393.4:n.6574+19C>A
NM_000132.3:c.6574+19C>A	NP_000123.1:n.6574+19C>A
NM_019863.2:c.169+19C>A	NP_063916.1:n.169+19C>A
XM_011531126.1:c.6469+19C>A	XP_011529428.1:n.6469+19C>A
NM_000132.4:c.6574+19C>A MANE Select	NP_000123.1:n.6574+19C>A
NM_019863.3:c.169+19C>A	NP_063916.1:n.169+19C>A