Canonical Allele Identifier: CA2466825982
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2072976877
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896040G>A , CM000685.2:g.154896040G>A GRCh38
NC_000023.10:g.154124315G>A , CM000685.1:g.154124315G>A GRCh37
NC_000023.9:g.153777509G>A NCBI36
NG_011403.1:g.131684C>T
NG_011403.2:g.131684C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6429+37C>T MANE Select ENSP00000353393.4:n.6429+37C>T
ENST00000360256.8:c.6429+37C>T ENSP00000353393.4:n.6429+37C>T
NM_000132.3:c.6429+37C>T NP_000123.1:n.6429+37C>T
XM_011531126.1:c.6324+37C>T XP_011529428.1:n.6324+37C>T
NM_000132.4:c.6429+37C>T MANE Select NP_000123.1:n.6429+37C>T
Search 100 bp 5'
Search 100 bp 3'