Canonical Allele Identifier: CA2695152807
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154901925-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154901925T>C , CM000685.2:g.154901925T>C GRCh38
NC_000023.10:g.154130200T>C , CM000685.1:g.154130200T>C GRCh37
NC_000023.9:g.153783394T>C NCBI36
NG_011403.1:g.125799A>G
NG_011403.2:g.125799A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6115+126A>G MANE Select ENSP00000353393.4:n.6115+126A>G
ENST00000360256.8:c.6115+126A>G ENSP00000353393.4:n.6115+126A>G
NM_000132.3:c.6115+126A>G NP_000123.1:n.6115+126A>G
XM_011531126.1:c.6010+126A>G XP_011529428.1:n.6010+126A>G
NM_000132.4:c.6115+126A>G MANE Select NP_000123.1:n.6115+126A>G
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