Canonical Allele Identifier: CA2695168784
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154928502-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928502T>G , CM000685.2:g.154928502T>G GRCh38
NC_000023.10:g.154156777T>G , CM000685.1:g.154156777T>G GRCh37
NC_000023.9:g.153809971T>G NCBI36
NG_011403.1:g.99222A>C
NG_011403.2:g.99222A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+69A>C MANE Select ENSP00000353393.4:n.5219+69A>C
ENST00000360256.8:c.5219+69A>C ENSP00000353393.4:n.5219+69A>C
NM_000132.3:c.5219+69A>C NP_000123.1:n.5219+69A>C
XM_011531126.1:c.5114+69A>C XP_011529428.1:n.5114+69A>C
NM_000132.4:c.5219+69A>C MANE Select NP_000123.1:n.5219+69A>C
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