Canonical Allele Identifier: CA2695168126
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904730G>T , CM000685.2:g.154904730G>T GRCh38
NC_000023.10:g.154133005G>T , CM000685.1:g.154133005G>T GRCh37
NC_000023.9:g.153786199G>T NCBI36
NG_011403.1:g.122994C>A
NG_011403.2:g.122994C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5586+81C>A MANE Select ENSP00000353393.4:n.5586+81C>A
ENST00000360256.8:c.5586+81C>A ENSP00000353393.4:n.5586+81C>A
NM_000132.3:c.5586+81C>A NP_000123.1:n.5586+81C>A
XM_011531126.1:c.5481+81C>A XP_011529428.1:n.5481+81C>A
NM_000132.4:c.5586+81C>A MANE Select NP_000123.1:n.5586+81C>A