Canonical Allele Identifier: CA2695169150
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154956900-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956900T>C , CM000685.2:g.154956900T>C GRCh38
NC_000023.10:g.154185175T>C , CM000685.1:g.154185175T>C GRCh37
NC_000023.9:g.153838369T>C NCBI36
NG_011403.1:g.70824A>G
NG_011403.2:g.70824A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1752+57A>G MANE Select ENSP00000353393.4:n.1752+57A>G
ENST00000647125.1:c.*1628+57A>G ENSP00000496062.1:n.*1628+57A>G
ENST00000360256.8:c.1752+57A>G ENSP00000353393.4:n.1752+57A>G
NM_000132.3:c.1752+57A>G NP_000123.1:n.1752+57A>G
XM_011531126.1:c.1647+57A>G XP_011529428.1:n.1647+57A>G
NM_000132.4:c.1752+57A>G MANE Select NP_000123.1:n.1752+57A>G
Search 100 bp 5'
Search 100 bp 3'