Canonical Allele Identifier: CA337319314

Gene: F8

Linked Data

• dbSNP Id: rs781966813
• gnomAD v3: X-154837495-C-A
• gnomAD v4: X-154837495-C-A
• MyVariant Identifiers: chrX:g.154065770C>A (hg19) ; chrX:g.154837495C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837495C>A , CM000685.2:g.154837495C>A	GRCh38
NC_000023.10:g.154065770C>A , CM000685.1:g.154065770C>A	GRCh37
NC_000023.9:g.153718964C>A	NCBI36
NG_011403.1:g.190229G>T
NG_033065.1:g.2168G>T
NG_011403.2:g.190229G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*102G>T MANE Select	ENSP00000353393.4:n.*102G>T
ENST00000644698.1:c.*102G>T	ENSP00000495706.1:n.*102G>T
ENST00000330287.10:c.*102G>T	ENSP00000327895.6:n.*102G>T
ENST00000360256.8:c.*102G>T	ENSP00000353393.4:n.*102G>T
NM_000132.3:c.*102G>T	NP_000123.1:n.*102G>T
NM_019863.2:c.*102G>T	NP_063916.1:n.*102G>T
XM_011531126.1:c.*102G>T	XP_011529428.1:n.*102G>T
NM_000132.4:c.*102G>T MANE Select	NP_000123.1:n.*102G>T
NM_019863.3:c.*102G>T	NP_063916.1:n.*102G>T