Canonical Allele Identifier: CA414908939
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904983T>G , CM000685.2:g.154904983T>G GRCh38
NC_000023.10:g.154133258T>G , CM000685.1:g.154133258T>G GRCh37
NC_000023.9:g.153786452T>G NCBI36
NG_011403.1:g.122741A>C
NG_011403.2:g.122741A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5414A>C MANE Select ENSP00000353393.4:p.Tyr1805Ser
ENST00000360256.8:c.5414A>C ENSP00000353393.4:p.Tyr1805Ser
NM_000132.3:c.5414A>C NP_000123.1:p.Tyr1805Ser
XM_011531126.1:c.5309A>C XP_011529428.1:p.Tyr1770Ser
NM_000132.4:c.5414A>C MANE Select NP_000123.1:p.Tyr1805Ser