Canonical Allele Identifier: CA414920019
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997042G>C , CM000685.2:g.154997042G>C GRCh38
NC_000023.10:g.154225317G>C , CM000685.1:g.154225317G>C GRCh37
NC_000023.9:g.153878511G>C NCBI36
NG_011403.1:g.30682C>G
NG_011403.2:g.30682C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.319C>G MANE Select ENSP00000353393.4:p.Leu107Val
ENST00000647125.1:c.*105C>G ENSP00000496062.1:n.*105C>G
ENST00000360256.8:c.319C>G ENSP00000353393.4:p.Leu107Val
ENST00000423959.5:c.214C>G ENSP00000409446.1:p.Leu72Val
ENST00000453950.1:c.301C>G ENSP00000389153.1:p.Leu101Val
NM_000132.3:c.319C>G NP_000123.1:p.Leu107Val
XM_011531126.1:c.214C>G XP_011529428.1:p.Leu72Val
NM_000132.4:c.319C>G MANE Select NP_000123.1:p.Leu107Val