Canonical Allele Identifier: CA2579744552
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904737T>C , CM000685.2:g.154904737T>C GRCh38
NC_000023.10:g.154133012T>C , CM000685.1:g.154133012T>C GRCh37
NC_000023.9:g.153786206T>C NCBI36
NG_011403.1:g.122987A>G
NG_011403.2:g.122987A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5586+74A>G MANE Select ENSP00000353393.4:n.5586+74A>G
ENST00000360256.8:c.5586+74A>G ENSP00000353393.4:n.5586+74A>G
NM_000132.3:c.5586+74A>G NP_000123.1:n.5586+74A>G
XM_011531126.1:c.5481+74A>G XP_011529428.1:n.5481+74A>G
NM_000132.4:c.5586+74A>G MANE Select NP_000123.1:n.5586+74A>G