Canonical Allele Identifier: CA519358665
Gene: F8 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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