Canonical Allele Identifier: CA519357898

Gene: F8

Linked Data

• dbSNP Id: rs1282595463
• gnomAD v2: X-154091431-G-A
• gnomAD v3: X-154863156-G-A
• gnomAD v4: X-154863156-G-A
• MyVariant Identifiers: chrX:g.154091431G>A (hg19) ; chrX:g.154863156G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863156G>A , CM000685.2:g.154863156G>A	GRCh38
NC_000023.10:g.154091431G>A , CM000685.1:g.154091431G>A	GRCh37
NC_000023.9:g.153744625G>A	NCBI36
NG_011403.1:g.164568C>T
NG_011403.2:g.164568C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6501C>T MANE Select	ENSP00000353393.4:p.Tyr2167=
ENST00000644698.1:c.234C>T	ENSP00000495706.1:p.Tyr78=
ENST00000330287.10:c.96C>T	ENSP00000327895.6:p.Tyr32=
ENST00000360256.8:c.6501C>T	ENSP00000353393.4:p.Tyr2167=
NM_000132.3:c.6501C>T	NP_000123.1:p.Tyr2167=
NM_019863.2:c.96C>T	NP_063916.1:p.Tyr32=
XM_011531126.1:c.6396C>T	XP_011529428.1:p.Tyr2132=
NM_000132.4:c.6501C>T MANE Select	NP_000123.1:p.Tyr2167=
NM_019863.3:c.96C>T	NP_063916.1:p.Tyr32=