Canonical Allele Identifier: CA414920687
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022526G>C , CM000685.2:g.155022526G>C GRCh38
NC_000023.10:g.154250801G>C , CM000685.1:g.154250801G>C GRCh37
NC_000023.9:g.153903995G>C NCBI36
NG_011403.1:g.5198C>G
NG_011403.2:g.5198C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.27C>G MANE Select ENSP00000353393.4:p.Phe9Leu
ENST00000647125.1:c.27C>G ENSP00000496062.1:p.Phe9Leu
ENST00000360256.8:c.27C>G ENSP00000353393.4:p.Phe9Leu
ENST00000423959.5:c.38+4254C>G ENSP00000409446.1:n.38+4254C>G
ENST00000453950.1:c.39-30C>G ENSP00000389153.1:n.39-30C>G
NM_000132.3:c.27C>G NP_000123.1:p.Phe9Leu
XM_011531126.1:c.38+4254C>G XP_011529428.1:n.38+4254C>G
NM_000132.4:c.27C>G MANE Select NP_000123.1:p.Phe9Leu