Canonical Allele Identifier: CA414914898
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928848G>T , CM000685.2:g.154928848G>T GRCh38
NC_000023.10:g.154157123G>T , CM000685.1:g.154157123G>T GRCh37
NC_000023.9:g.153810317G>T NCBI36
NG_011403.1:g.98876C>A
NG_011403.2:g.98876C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4942C>A MANE Select ENSP00000353393.4:p.Gln1648Lys
ENST00000360256.8:c.4942C>A ENSP00000353393.4:p.Gln1648Lys
NM_000132.3:c.4942C>A NP_000123.1:p.Gln1648Lys
XM_011531126.1:c.4837C>A XP_011529428.1:p.Gln1613Lys
NM_000132.4:c.4942C>A MANE Select NP_000123.1:p.Gln1648Lys