Canonical Allele Identifier: CA414910673
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1426450176

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953945G>A , CM000685.2:g.154953945G>A GRCh38
NC_000023.10:g.154182220G>A , CM000685.1:g.154182220G>A GRCh37
NC_000023.9:g.153835414G>A NCBI36
NG_011403.1:g.73779C>T
NG_011403.2:g.73779C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1850C>T MANE Select ENSP00000353393.4:p.Pro617Leu
ENST00000647125.1:c.*1726C>T ENSP00000496062.1:n.*1726C>T
ENST00000360256.8:c.1850C>T ENSP00000353393.4:p.Pro617Leu
NM_000132.3:c.1850C>T NP_000123.1:p.Pro617Leu
XM_011531126.1:c.1745C>T XP_011529428.1:p.Pro582Leu
NM_000132.4:c.1850C>T MANE Select NP_000123.1:p.Pro617Leu