Canonical Allele Identifier: CA414908900
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154133251G>T (hg19) chrX:g.154904976G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904976G>T , CM000685.2:g.154904976G>T GRCh38
NC_000023.10:g.154133251G>T , CM000685.1:g.154133251G>T GRCh37
NC_000023.9:g.153786445G>T NCBI36
NG_011403.1:g.122748C>A
NG_011403.2:g.122748C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5421C>A MANE Select ENSP00000353393.4:p.Ser1807Arg
ENST00000360256.8:c.5421C>A ENSP00000353393.4:p.Ser1807Arg
NM_000132.3:c.5421C>A NP_000123.1:p.Ser1807Arg
XM_011531126.1:c.5316C>A XP_011529428.1:p.Ser1772Arg
NM_000132.4:c.5421C>A MANE Select NP_000123.1:p.Ser1807Arg
Search 100 bp 5'
Search 100 bp 3'