Canonical Allele Identifier: CA414902893
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860439T>C , CM000685.2:g.154860439T>C GRCh38
NC_000023.10:g.154088714T>C , CM000685.1:g.154088714T>C GRCh37
NC_000023.9:g.153741908T>C NCBI36
NG_011403.1:g.167285A>G
NG_011403.2:g.167285A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6893A>G MANE Select ENSP00000353393.4:p.Lys2298Arg
ENST00000644698.1:c.626A>G ENSP00000495706.1:p.Lys209Arg
ENST00000330287.10:c.488A>G ENSP00000327895.6:p.Lys163Arg
ENST00000360256.8:c.6893A>G ENSP00000353393.4:p.Lys2298Arg
NM_000132.3:c.6893A>G NP_000123.1:p.Lys2298Arg
NM_019863.2:c.488A>G NP_063916.1:p.Lys163Arg
XM_011531126.1:c.6788A>G XP_011529428.1:p.Lys2263Arg
NM_000132.4:c.6893A>G MANE Select NP_000123.1:p.Lys2298Arg
NM_019863.3:c.488A>G NP_063916.1:p.Lys163Arg