Canonical Allele Identifier: CA414903638
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860503T>C , CM000685.2:g.154860503T>C GRCh38
NC_000023.10:g.154088778T>C , CM000685.1:g.154088778T>C GRCh37
NC_000023.9:g.153741972T>C NCBI36
NG_011403.1:g.167221A>G
NG_011403.2:g.167221A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6829A>G MANE Select ENSP00000353393.4:p.Lys2277Glu
ENST00000644698.1:c.562A>G ENSP00000495706.1:p.Lys188Glu
ENST00000330287.10:c.424A>G ENSP00000327895.6:p.Lys142Glu
ENST00000360256.8:c.6829A>G ENSP00000353393.4:p.Lys2277Glu
NM_000132.3:c.6829A>G NP_000123.1:p.Lys2277Glu
NM_019863.2:c.424A>G NP_063916.1:p.Lys142Glu
XM_011531126.1:c.6724A>G XP_011529428.1:p.Lys2242Glu
NM_000132.4:c.6829A>G MANE Select NP_000123.1:p.Lys2277Glu
NM_019863.3:c.424A>G NP_063916.1:p.Lys142Glu