Canonical Allele Identifier: CA2579744394
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896041T>A , CM000685.2:g.154896041T>A GRCh38
NC_000023.10:g.154124316T>A , CM000685.1:g.154124316T>A GRCh37
NC_000023.9:g.153777510T>A NCBI36
NG_011403.1:g.131683A>T
NG_011403.2:g.131683A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6429+36A>T MANE Select ENSP00000353393.4:n.6429+36A>T
ENST00000360256.8:c.6429+36A>T ENSP00000353393.4:n.6429+36A>T
NM_000132.3:c.6429+36A>T NP_000123.1:n.6429+36A>T
XM_011531126.1:c.6324+36A>T XP_011529428.1:n.6324+36A>T
NM_000132.4:c.6429+36A>T MANE Select NP_000123.1:n.6429+36A>T
Search 100 bp 5'
Search 100 bp 3'