Canonical Allele Identifier: CA519357746
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154182225G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953950G>T , CM000685.2:g.154953950G>T GRCh38
NC_000023.10:g.154182225G>T , CM000685.1:g.154182225G>T GRCh37
NC_000023.9:g.153835419G>T NCBI36
NG_011403.1:g.73774C>A
NG_011403.2:g.73774C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1845C>A MANE Select ENSP00000353393.4:p.Pro615=
ENST00000647125.1:c.*1721C>A ENSP00000496062.1:n.*1721C>A
ENST00000360256.8:c.1845C>A ENSP00000353393.4:p.Pro615=
NM_000132.3:c.1845C>A NP_000123.1:p.Pro615=
XM_011531126.1:c.1740C>A XP_011529428.1:p.Pro580=
NM_000132.4:c.1845C>A MANE Select NP_000123.1:p.Pro615=