Canonical Allele Identifier: CA414907850
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863195T>C , CM000685.2:g.154863195T>C GRCh38
NC_000023.10:g.154091470T>C , CM000685.1:g.154091470T>C GRCh37
NC_000023.9:g.153744664T>C NCBI36
NG_011403.1:g.164529A>G
NG_011403.2:g.164529A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6462A>G MANE Select ENSP00000353393.4:p.Ile2154Met
ENST00000644698.1:c.195A>G ENSP00000495706.1:p.Ile65Met
ENST00000330287.10:c.57A>G ENSP00000327895.6:p.Ile19Met
ENST00000360256.8:c.6462A>G ENSP00000353393.4:p.Ile2154Met
NM_000132.3:c.6462A>G NP_000123.1:p.Ile2154Met
NM_019863.2:c.57A>G NP_063916.1:p.Ile19Met
XM_011531126.1:c.6357A>G XP_011529428.1:p.Ile2119Met
NM_000132.4:c.6462A>G MANE Select NP_000123.1:p.Ile2154Met
NM_019863.3:c.57A>G NP_063916.1:p.Ile19Met