Canonical Allele Identifier: CA414897650
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837728A>G , CM000685.2:g.154837728A>G GRCh38
NC_000023.10:g.154066003A>G , CM000685.1:g.154066003A>G GRCh37
NC_000023.9:g.153719197A>G NCBI36
NG_011403.1:g.189996T>C
NG_033065.1:g.1935T>C
NG_011403.2:g.189996T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6925T>C MANE Select ENSP00000353393.4:p.Phe2309Leu
ENST00000644698.1:c.658T>C ENSP00000495706.1:p.Phe220Leu
ENST00000330287.10:c.520T>C ENSP00000327895.6:p.Phe174Leu
ENST00000360256.8:c.6925T>C ENSP00000353393.4:p.Phe2309Leu
NM_000132.3:c.6925T>C NP_000123.1:p.Phe2309Leu
NM_019863.2:c.520T>C NP_063916.1:p.Phe174Leu
XM_011531126.1:c.6820T>C XP_011529428.1:p.Phe2274Leu
NM_000132.4:c.6925T>C MANE Select NP_000123.1:p.Phe2309Leu
NM_019863.3:c.520T>C NP_063916.1:p.Phe174Leu