Canonical Allele Identifier: CA645292779
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1339446588

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904704C>T , CM000685.2:g.154904704C>T GRCh38
NC_000023.10:g.154132979C>T , CM000685.1:g.154132979C>T GRCh37
NC_000023.9:g.153786173C>T NCBI36
NG_011403.1:g.123020G>A
NG_011403.2:g.123020G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5586+107G>A MANE Select ENSP00000353393.4:n.5586+107G>A
ENST00000360256.8:c.5586+107G>A ENSP00000353393.4:n.5586+107G>A
NM_000132.3:c.5586+107G>A NP_000123.1:n.5586+107G>A
XM_011531126.1:c.5481+107G>A XP_011529428.1:n.5481+107G>A
NM_000132.4:c.5586+107G>A MANE Select NP_000123.1:n.5586+107G>A