Canonical Allele Identifier: CA2695169250
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154960984-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154960984A>G , CM000685.2:g.154960984A>G GRCh38
NC_000023.10:g.154189259A>G , CM000685.1:g.154189259A>G GRCh37
NC_000023.9:g.153842453A>G NCBI36
NG_011403.1:g.66740T>C
NG_011403.2:g.66740T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1537+91T>C MANE Select ENSP00000353393.4:n.1537+91T>C
ENST00000647125.1:c.*1413+91T>C ENSP00000496062.1:n.*1413+91T>C
ENST00000360256.8:c.1537+91T>C ENSP00000353393.4:n.1537+91T>C
NM_000132.3:c.1537+91T>C NP_000123.1:n.1537+91T>C
XM_011531126.1:c.1432+91T>C XP_011529428.1:n.1432+91T>C
NM_000132.4:c.1537+91T>C MANE Select NP_000123.1:n.1537+91T>C
Search 100 bp 5'
Search 100 bp 3'