Canonical Allele Identifier: CA2695152852
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154901984-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154901984G>T , CM000685.2:g.154901984G>T GRCh38
NC_000023.10:g.154130259G>T , CM000685.1:g.154130259G>T GRCh37
NC_000023.9:g.153783453G>T NCBI36
NG_011403.1:g.125740C>A
NG_011403.2:g.125740C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6115+67C>A MANE Select ENSP00000353393.4:n.6115+67C>A
ENST00000360256.8:c.6115+67C>A ENSP00000353393.4:n.6115+67C>A
NM_000132.3:c.6115+67C>A NP_000123.1:n.6115+67C>A
XM_011531126.1:c.6010+67C>A XP_011529428.1:n.6010+67C>A
NM_000132.4:c.6115+67C>A MANE Select NP_000123.1:n.6115+67C>A
Search 100 bp 5'
Search 100 bp 3'