Canonical Allele Identifier: CA414900382
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896226G>T , CM000685.2:g.154896226G>T GRCh38
NC_000023.10:g.154124501G>T , CM000685.1:g.154124501G>T GRCh37
NC_000023.9:g.153777695G>T NCBI36
NG_011403.1:g.131498C>A
NG_011403.2:g.131498C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6280C>A MANE Select ENSP00000353393.4:p.Leu2094Met
ENST00000360256.8:c.6280C>A ENSP00000353393.4:p.Leu2094Met
NM_000132.3:c.6280C>A NP_000123.1:p.Leu2094Met
XM_011531126.1:c.6175C>A XP_011529428.1:p.Leu2059Met
NM_000132.4:c.6280C>A MANE Select NP_000123.1:p.Leu2094Met