Canonical Allele Identifier: CA414906056
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132273T>A (hg19) chrX:g.154903998T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903998T>A , CM000685.2:g.154903998T>A GRCh38
NC_000023.10:g.154132273T>A , CM000685.1:g.154132273T>A GRCh37
NC_000023.9:g.153785467T>A NCBI36
NG_011403.1:g.123726A>T
NG_011403.2:g.123726A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5906A>T MANE Select ENSP00000353393.4:p.Asn1969Ile
ENST00000360256.8:c.5906A>T ENSP00000353393.4:p.Asn1969Ile
NM_000132.3:c.5906A>T NP_000123.1:p.Asn1969Ile
XM_011531126.1:c.5801A>T XP_011529428.1:p.Asn1934Ile
NM_000132.4:c.5906A>T MANE Select NP_000123.1:p.Asn1969Ile
Search 100 bp 5'
Search 100 bp 3'