Canonical Allele Identifier: CA2466835699
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073171643
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928486C>T , CM000685.2:g.154928486C>T GRCh38
NC_000023.10:g.154156761C>T , CM000685.1:g.154156761C>T GRCh37
NC_000023.9:g.153809955C>T NCBI36
NG_011403.1:g.99238G>A
NG_011403.2:g.99238G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+85G>A MANE Select ENSP00000353393.4:n.5219+85G>A
ENST00000360256.8:c.5219+85G>A ENSP00000353393.4:n.5219+85G>A
NM_000132.3:c.5219+85G>A NP_000123.1:n.5219+85G>A
XM_011531126.1:c.5114+85G>A XP_011529428.1:n.5114+85G>A
NM_000132.4:c.5219+85G>A MANE Select NP_000123.1:n.5219+85G>A
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