Canonical Allele Identifier: CA414896790

Gene: F8

Linked Data

• gnomAD v4: X-154837635-T-A
• MyVariant Identifiers: chrX:g.154065910T>A (hg19) ; chrX:g.154837635T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837635T>A , CM000685.2:g.154837635T>A	GRCh38
NC_000023.10:g.154065910T>A , CM000685.1:g.154065910T>A	GRCh37
NC_000023.9:g.153719104T>A	NCBI36
NG_011403.1:g.190089A>T
NG_033065.1:g.2028A>T
NG_011403.2:g.190089A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7018A>T MANE Select	ENSP00000353393.4:p.Met2340Leu
ENST00000644698.1:c.751A>T	ENSP00000495706.1:p.Met251Leu
ENST00000330287.10:c.613A>T	ENSP00000327895.6:p.Met205Leu
ENST00000360256.8:c.7018A>T	ENSP00000353393.4:p.Met2340Leu
NM_000132.3:c.7018A>T	NP_000123.1:p.Met2340Leu
NM_019863.2:c.613A>T	NP_063916.1:p.Met205Leu
XM_011531126.1:c.6913A>T	XP_011529428.1:p.Met2305Leu
NM_000132.4:c.7018A>T MANE Select	NP_000123.1:p.Met2340Leu
NM_019863.3:c.613A>T	NP_063916.1:p.Met205Leu