Canonical Allele Identifier: CA414907269
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863133T>A , CM000685.2:g.154863133T>A GRCh38
NC_000023.10:g.154091408T>A , CM000685.1:g.154091408T>A GRCh37
NC_000023.9:g.153744602T>A NCBI36
NG_011403.1:g.164591A>T
NG_011403.2:g.164591A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6524A>T MANE Select ENSP00000353393.4:p.Tyr2175Phe
ENST00000644698.1:c.257A>T ENSP00000495706.1:p.Tyr86Phe
ENST00000330287.10:c.119A>T ENSP00000327895.6:p.Tyr40Phe
ENST00000360256.8:c.6524A>T ENSP00000353393.4:p.Tyr2175Phe
NM_000132.3:c.6524A>T NP_000123.1:p.Tyr2175Phe
NM_019863.2:c.119A>T NP_063916.1:p.Tyr40Phe
XM_011531126.1:c.6419A>T XP_011529428.1:p.Tyr2140Phe
NM_000132.4:c.6524A>T MANE Select NP_000123.1:p.Tyr2175Phe
NM_019863.3:c.119A>T NP_063916.1:p.Tyr40Phe