Canonical Allele Identifier: CA414907860
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863197T>G , CM000685.2:g.154863197T>G GRCh38
NC_000023.10:g.154091472T>G , CM000685.1:g.154091472T>G GRCh37
NC_000023.9:g.153744666T>G NCBI36
NG_011403.1:g.164527A>C
NG_011403.2:g.164527A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6460A>C MANE Select ENSP00000353393.4:p.Ile2154Leu
ENST00000644698.1:c.193A>C ENSP00000495706.1:p.Ile65Leu
ENST00000330287.10:c.55A>C ENSP00000327895.6:p.Ile19Leu
ENST00000360256.8:c.6460A>C ENSP00000353393.4:p.Ile2154Leu
NM_000132.3:c.6460A>C NP_000123.1:p.Ile2154Leu
NM_019863.2:c.55A>C NP_063916.1:p.Ile19Leu
XM_011531126.1:c.6355A>C XP_011529428.1:p.Ile2119Leu
NM_000132.4:c.6460A>C MANE Select NP_000123.1:p.Ile2154Leu
NM_019863.3:c.55A>C NP_063916.1:p.Ile19Leu