Canonical Allele Identifier: CA10567719

Gene: F8

Linked Data

• dbSNP Id: rs201147256
• ExAC: X:154065851 C / T
• gnomAD v2: X-154065851-C-T
• gnomAD v3: X-154837576-C-T
• gnomAD v4: X-154837576-C-T
• MyVariant Identifiers: chrX:g.154065851C>T (hg19) ; chrX:g.154837576C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837576C>T , CM000685.2:g.154837576C>T	GRCh38
NC_000023.10:g.154065851C>T , CM000685.1:g.154065851C>T	GRCh37
NC_000023.9:g.153719045C>T	NCBI36
NG_011403.1:g.190148G>A
NG_033065.1:g.2087G>A
NG_011403.2:g.190148G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*21G>A MANE Select	ENSP00000353393.4:n.*21G>A
ENST00000644698.1:c.*21G>A	ENSP00000495706.1:n.*21G>A
ENST00000330287.10:c.*21G>A	ENSP00000327895.6:n.*21G>A
ENST00000360256.8:c.*21G>A	ENSP00000353393.4:n.*21G>A
NM_000132.3:c.*21G>A	NP_000123.1:n.*21G>A
NM_019863.2:c.*21G>A	NP_063916.1:n.*21G>A
XM_011531126.1:c.*21G>A	XP_011529428.1:n.*21G>A
NM_000132.4:c.*21G>A MANE Select	NP_000123.1:n.*21G>A
NM_019863.3:c.*21G>A	NP_063916.1:n.*21G>A