Canonical Allele Identifier: CA1138603009
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073445273
gnomAD v3: X-154969556-T-G
gnomAD v4: X-154969556-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969556T>G , CM000685.2:g.154969556T>G GRCh38
NC_000023.10:g.154197831T>G , CM000685.1:g.154197831T>G GRCh37
NC_000023.9:g.153851025T>G NCBI36
NG_011403.1:g.58168A>C
NG_011403.2:g.58168A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.788-4A>C MANE Select ENSP00000353393.4:n.788-4A>C
ENST00000647125.1:c.*664-4A>C ENSP00000496062.1:n.*664-4A>C
ENST00000360256.8:c.788-4A>C ENSP00000353393.4:n.788-4A>C
NM_000132.3:c.788-4A>C NP_000123.1:n.788-4A>C
XM_011531126.1:c.683-4A>C XP_011529428.1:n.683-4A>C
NM_000132.4:c.788-4A>C MANE Select NP_000123.1:n.788-4A>C
Search 100 bp 5'
Search 100 bp 3'