Canonical Allele Identifier: CA873367581

Gene: F8

Linked Data

• dbSNP Id: rs1378144931
• gnomAD v3: X-155022720-A-G
• gnomAD v4: X-155022720-A-G
• MyVariant Identifiers: chrX:g.155022720A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022720A>G , CM000685.2:g.155022720A>G	GRCh38
NC_000023.10:g.154250995A>G , CM000685.1:g.154250995A>G	GRCh37
NC_000023.9:g.153904189A>G	NCBI36
NG_011403.1:g.5004T>C
NG_011403.2:g.5004T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-168T>C MANE Select	ENSP00000353393.4:n.-168T>C
ENST00000360256.8:c.-168T>C	ENSP00000353393.4:n.-168T>C
ENST00000423959.5:c.38+4060T>C	ENSP00000409446.1:n.38+4060T>C
ENST00000453950.1:c.39-224T>C	ENSP00000389153.1:n.39-224T>C
NM_000132.3:c.-168T>C	NP_000123.1:n.-168T>C
XM_011531126.1:c.38+4060T>C	XP_011529428.1:n.38+4060T>C
NM_000132.4:c.-168T>C MANE Select	NP_000123.1:n.-168T>C