Canonical Allele Identifier: CA873367564

Gene: F8

Linked Data

• dbSNP Id: rs1257471250
• gnomAD v4: X-155022665-C-A
• MyVariant Identifiers: chrX:g.155022665C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022665C>A , CM000685.2:g.155022665C>A	GRCh38
NC_000023.10:g.154250940C>A , CM000685.1:g.154250940C>A	GRCh37
NC_000023.9:g.153904134C>A	NCBI36
NG_011403.1:g.5059G>T
NG_011403.2:g.5059G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-113G>T MANE Select	ENSP00000353393.4:n.-113G>T
ENST00000647125.1:c.-113G>T	ENSP00000496062.1:n.-113G>T
ENST00000360256.8:c.-113G>T	ENSP00000353393.4:n.-113G>T
ENST00000423959.5:c.38+4115G>T	ENSP00000409446.1:n.38+4115G>T
ENST00000453950.1:c.39-169G>T	ENSP00000389153.1:n.39-169G>T
NM_000132.3:c.-113G>T	NP_000123.1:n.-113G>T
XM_011531126.1:c.38+4115G>T	XP_011529428.1:n.38+4115G>T
NM_000132.4:c.-113G>T MANE Select	NP_000123.1:n.-113G>T