Canonical Allele Identifier: CA2824302188
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928451C>G , CM000685.2:g.154928451C>G GRCh38
NC_000023.10:g.154156726C>G , CM000685.1:g.154156726C>G GRCh37
NC_000023.9:g.153809920C>G NCBI36
NG_011403.1:g.99273G>C
NG_011403.2:g.99273G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+120G>C MANE Select ENSP00000353393.4:n.5219+120G>C
ENST00000360256.8:c.5219+120G>C ENSP00000353393.4:n.5219+120G>C
NM_000132.3:c.5219+120G>C NP_000123.1:n.5219+120G>C
XM_011531126.1:c.5114+120G>C XP_011529428.1:n.5114+120G>C
NM_000132.4:c.5219+120G>C MANE Select NP_000123.1:n.5219+120G>C
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