Canonical Allele Identifier: CA2466828384
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073028772

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904700T>G , CM000685.2:g.154904700T>G GRCh38
NC_000023.10:g.154132975T>G , CM000685.1:g.154132975T>G GRCh37
NC_000023.9:g.153786169T>G NCBI36
NG_011403.1:g.123024A>C
NG_011403.2:g.123024A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5586+111A>C MANE Select ENSP00000353393.4:n.5586+111A>C
ENST00000360256.8:c.5586+111A>C ENSP00000353393.4:n.5586+111A>C
NM_000132.3:c.5586+111A>C NP_000123.1:n.5586+111A>C
XM_011531126.1:c.5481+111A>C XP_011529428.1:n.5481+111A>C
NM_000132.4:c.5586+111A>C MANE Select NP_000123.1:n.5586+111A>C