Canonical Allele Identifier: CA2695168750
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154928419-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928419C>T , CM000685.2:g.154928419C>T GRCh38
NC_000023.10:g.154156694C>T , CM000685.1:g.154156694C>T GRCh37
NC_000023.9:g.153809888C>T NCBI36
NG_011403.1:g.99305G>A
NG_011403.2:g.99305G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5219+152G>A MANE Select ENSP00000353393.4:n.5219+152G>A
ENST00000360256.8:c.5219+152G>A ENSP00000353393.4:n.5219+152G>A
NM_000132.3:c.5219+152G>A NP_000123.1:n.5219+152G>A
XM_011531126.1:c.5114+152G>A XP_011529428.1:n.5114+152G>A
NM_000132.4:c.5219+152G>A MANE Select NP_000123.1:n.5219+152G>A
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