Canonical Allele Identifier: CA414907257
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863132A>T , CM000685.2:g.154863132A>T GRCh38
NC_000023.10:g.154091407A>T , CM000685.1:g.154091407A>T GRCh37
NC_000023.9:g.153744601A>T NCBI36
NG_011403.1:g.164592T>A
NG_011403.2:g.164592T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6525T>A MANE Select ENSP00000353393.4:p.Tyr2175Ter
ENST00000644698.1:c.258T>A ENSP00000495706.1:p.Tyr86Ter
ENST00000330287.10:c.120T>A ENSP00000327895.6:p.Tyr40Ter
ENST00000360256.8:c.6525T>A ENSP00000353393.4:p.Tyr2175Ter
NM_000132.3:c.6525T>A NP_000123.1:p.Tyr2175Ter
NM_019863.2:c.120T>A NP_063916.1:p.Tyr40Ter
XM_011531126.1:c.6420T>A XP_011529428.1:p.Tyr2140Ter
NM_000132.4:c.6525T>A MANE Select NP_000123.1:p.Tyr2175Ter
NM_019863.3:c.120T>A NP_063916.1:p.Tyr40Ter