Canonical Allele Identifier: CA519357812
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154091377C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863102C>T , CM000685.2:g.154863102C>T GRCh38
NC_000023.10:g.154091377C>T , CM000685.1:g.154091377C>T GRCh37
NC_000023.9:g.153744571C>T NCBI36
NG_011403.1:g.164622G>A
NG_011403.2:g.164622G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6555G>A MANE Select ENSP00000353393.4:p.Leu2185=
ENST00000644698.1:c.288G>A ENSP00000495706.1:p.Leu96=
ENST00000330287.10:c.150G>A ENSP00000327895.6:p.Leu50=
ENST00000360256.8:c.6555G>A ENSP00000353393.4:p.Leu2185=
NM_000132.3:c.6555G>A NP_000123.1:p.Leu2185=
NM_019863.2:c.150G>A NP_063916.1:p.Leu50=
XM_011531126.1:c.6450G>A XP_011529428.1:p.Leu2150=
NM_000132.4:c.6555G>A MANE Select NP_000123.1:p.Leu2185=
NM_019863.3:c.150G>A NP_063916.1:p.Leu50=