Canonical Allele Identifier: CA873369315

Gene: F8

Linked Data

• dbSNP Id: rs1436873837
• gnomAD v3: X-154862993-A-G
• gnomAD v4: X-154862993-A-G
• MyVariant Identifiers: chrX:g.154862993A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154862993A>G , CM000685.2:g.154862993A>G	GRCh38
NC_000023.10:g.154091268A>G , CM000685.1:g.154091268A>G	GRCh37
NC_000023.9:g.153744462A>G	NCBI36
NG_011403.1:g.164731T>C
NG_011403.2:g.164731T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6574+90T>C MANE Select	ENSP00000353393.4:n.6574+90T>C
ENST00000644698.1:c.307+90T>C	ENSP00000495706.1:n.307+90T>C
ENST00000330287.10:c.169+90T>C	ENSP00000327895.6:n.169+90T>C
ENST00000360256.8:c.6574+90T>C	ENSP00000353393.4:n.6574+90T>C
NM_000132.3:c.6574+90T>C	NP_000123.1:n.6574+90T>C
NM_019863.2:c.169+90T>C	NP_063916.1:n.169+90T>C
XM_011531126.1:c.6469+90T>C	XP_011529428.1:n.6469+90T>C
NM_000132.4:c.6574+90T>C MANE Select	NP_000123.1:n.6574+90T>C
NM_019863.3:c.169+90T>C	NP_063916.1:n.169+90T>C