Canonical Allele Identifier: CA519356238
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1236707560

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860546T>C , CM000685.2:g.154860546T>C GRCh38
NC_000023.10:g.154088821T>C , CM000685.1:g.154088821T>C GRCh37
NC_000023.9:g.153742015T>C NCBI36
NG_011403.1:g.167178A>G
NG_011403.2:g.167178A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6786A>G MANE Select ENSP00000353393.4:p.Val2262=
ENST00000644698.1:c.519A>G ENSP00000495706.1:p.Val173=
ENST00000330287.10:c.381A>G ENSP00000327895.6:p.Val127=
ENST00000360256.8:c.6786A>G ENSP00000353393.4:p.Val2262=
NM_000132.3:c.6786A>G NP_000123.1:p.Val2262=
NM_019863.2:c.381A>G NP_063916.1:p.Val127=
XM_011531126.1:c.6681A>G XP_011529428.1:p.Val2227=
NM_000132.4:c.6786A>G MANE Select NP_000123.1:p.Val2262=
NM_019863.3:c.381A>G NP_063916.1:p.Val127=