Canonical Allele Identifier: CA414910688
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953947A>C , CM000685.2:g.154953947A>C GRCh38
NC_000023.10:g.154182222A>C , CM000685.1:g.154182222A>C GRCh37
NC_000023.9:g.153835416A>C NCBI36
NG_011403.1:g.73777T>G
NG_011403.2:g.73777T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1848T>G MANE Select ENSP00000353393.4:p.Asn616Lys
ENST00000647125.1:c.*1724T>G ENSP00000496062.1:n.*1724T>G
ENST00000360256.8:c.1848T>G ENSP00000353393.4:p.Asn616Lys
NM_000132.3:c.1848T>G NP_000123.1:p.Asn616Lys
XM_011531126.1:c.1743T>G XP_011529428.1:p.Asn581Lys
NM_000132.4:c.1848T>G MANE Select NP_000123.1:p.Asn616Lys