Canonical Allele Identifier: CA519358661
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154185349A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957074A>T , CM000685.2:g.154957074A>T GRCh38
NC_000023.10:g.154185349A>T , CM000685.1:g.154185349A>T GRCh37
NC_000023.9:g.153838543A>T NCBI36
NG_011403.1:g.70650T>A
NG_011403.2:g.70650T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1635T>A MANE Select ENSP00000353393.4:p.Pro545=
ENST00000647125.1:c.*1511T>A ENSP00000496062.1:n.*1511T>A
ENST00000360256.8:c.1635T>A ENSP00000353393.4:p.Pro545=
NM_000132.3:c.1635T>A NP_000123.1:p.Pro545=
XM_011531126.1:c.1530T>A XP_011529428.1:p.Pro510=
NM_000132.4:c.1635T>A MANE Select NP_000123.1:p.Pro545=