Canonical Allele Identifier: CA414909234
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154947762A>C , CM000685.2:g.154947762A>C GRCh38
NC_000023.10:g.154176037A>C , CM000685.1:g.154176037A>C GRCh37
NC_000023.9:g.153829231A>C NCBI36
NG_011403.1:g.79962T>G
NG_011403.2:g.79962T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.2049T>G MANE Select ENSP00000353393.4:p.Tyr683Ter
ENST00000647125.1:c.*1779+6130T>G ENSP00000496062.1:n.*1779+6130T>G
ENST00000360256.8:c.2049T>G ENSP00000353393.4:p.Tyr683Ter
NM_000132.3:c.2049T>G NP_000123.1:p.Tyr683Ter
XM_011531126.1:c.1944T>G XP_011529428.1:p.Tyr648Ter
NM_000132.4:c.2049T>G MANE Select NP_000123.1:p.Tyr683Ter