Canonical Allele Identifier: CA414917743
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969377G>C , CM000685.2:g.154969377G>C GRCh38
NC_000023.10:g.154197652G>C , CM000685.1:g.154197652G>C GRCh37
NC_000023.9:g.153850846G>C NCBI36
NG_011403.1:g.58347C>G
NG_011403.2:g.58347C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.963C>G MANE Select ENSP00000353393.4:p.Asp321Glu
ENST00000647125.1:c.*839C>G ENSP00000496062.1:n.*839C>G
ENST00000360256.8:c.963C>G ENSP00000353393.4:p.Asp321Glu
NM_000132.3:c.963C>G NP_000123.1:p.Asp321Glu
XM_011531126.1:c.858C>G XP_011529428.1:p.Asp286Glu
NM_000132.4:c.963C>G MANE Select NP_000123.1:p.Asp321Glu