Canonical Allele Identifier: CA414910676
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1850C>G MANE Select ENSP00000353393.4:p.Pro617Arg
ENST00000647125.1:c.*1726C>G ENSP00000496062.1:n.*1726C>G
ENST00000360256.8:c.1850C>G ENSP00000353393.4:p.Pro617Arg
NM_000132.3:c.1850C>G NP_000123.1:p.Pro617Arg
XM_011531126.1:c.1745C>G XP_011529428.1:p.Pro582Arg
NM_000132.4:c.1850C>G MANE Select NP_000123.1:p.Pro617Arg