Canonical Allele Identifier: CA414917764
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969381A>T , CM000685.2:g.154969381A>T GRCh38
NC_000023.10:g.154197656A>T , CM000685.1:g.154197656A>T GRCh37
NC_000023.9:g.153850850A>T NCBI36
NG_011403.1:g.58343T>A
NG_011403.2:g.58343T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.959T>A MANE Select ENSP00000353393.4:p.Met320Lys
ENST00000647125.1:c.*835T>A ENSP00000496062.1:n.*835T>A
ENST00000360256.8:c.959T>A ENSP00000353393.4:p.Met320Lys
NM_000132.3:c.959T>A NP_000123.1:p.Met320Lys
XM_011531126.1:c.854T>A XP_011529428.1:p.Met285Lys
NM_000132.4:c.959T>A MANE Select NP_000123.1:p.Met320Lys