Canonical Allele Identifier: CA2466825988
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2072976989
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896059A>T , CM000685.2:g.154896059A>T GRCh38
NC_000023.10:g.154124334A>T , CM000685.1:g.154124334A>T GRCh37
NC_000023.9:g.153777528A>T NCBI36
NG_011403.1:g.131665T>A
NG_011403.2:g.131665T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6429+18T>A MANE Select ENSP00000353393.4:n.6429+18T>A
ENST00000360256.8:c.6429+18T>A ENSP00000353393.4:n.6429+18T>A
NM_000132.3:c.6429+18T>A NP_000123.1:n.6429+18T>A
XM_011531126.1:c.6324+18T>A XP_011529428.1:n.6324+18T>A
NM_000132.4:c.6429+18T>A MANE Select NP_000123.1:n.6429+18T>A
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