Canonical Allele Identifier: CA10567720
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782115089

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837580T>G , CM000685.2:g.154837580T>G GRCh38
NC_000023.10:g.154065855T>G , CM000685.1:g.154065855T>G GRCh37
NC_000023.9:g.153719049T>G NCBI36
NG_011403.1:g.190144A>C
NG_033065.1:g.2083A>C
NG_011403.2:g.190144A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*17A>C MANE Select ENSP00000353393.4:n.*17A>C
ENST00000644698.1:c.*17A>C ENSP00000495706.1:n.*17A>C
ENST00000330287.10:c.*17A>C ENSP00000327895.6:n.*17A>C
ENST00000360256.8:c.*17A>C ENSP00000353393.4:n.*17A>C
NM_000132.3:c.*17A>C NP_000123.1:n.*17A>C
NM_019863.2:c.*17A>C NP_063916.1:n.*17A>C
XM_011531126.1:c.*17A>C XP_011529428.1:n.*17A>C
NM_000132.4:c.*17A>C MANE Select NP_000123.1:n.*17A>C
NM_019863.3:c.*17A>C NP_063916.1:n.*17A>C