Canonical Allele Identifier: CA2695153023
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903886G>T , CM000685.2:g.154903886G>T GRCh38
NC_000023.10:g.154132161G>T , CM000685.1:g.154132161G>T GRCh37
NC_000023.9:g.153785355G>T NCBI36
NG_011403.1:g.123838C>A
NG_011403.2:g.123838C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5998+20C>A MANE Select ENSP00000353393.4:n.5998+20C>A
ENST00000360256.8:c.5998+20C>A ENSP00000353393.4:n.5998+20C>A
NM_000132.3:c.5998+20C>A NP_000123.1:n.5998+20C>A
XM_011531126.1:c.5893+20C>A XP_011529428.1:n.5893+20C>A
NM_000132.4:c.5998+20C>A MANE Select NP_000123.1:n.5998+20C>A