Canonical Allele Identifier: CA414899746
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154124422A>T (hg19) chrX:g.154896147A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896147A>T , CM000685.2:g.154896147A>T GRCh38
NC_000023.10:g.154124422A>T , CM000685.1:g.154124422A>T GRCh37
NC_000023.9:g.153777616A>T NCBI36
NG_011403.1:g.131577T>A
NG_011403.2:g.131577T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6359T>A MANE Select ENSP00000353393.4:p.Phe2120Tyr
ENST00000360256.8:c.6359T>A ENSP00000353393.4:p.Phe2120Tyr
NM_000132.3:c.6359T>A NP_000123.1:p.Phe2120Tyr
XM_011531126.1:c.6254T>A XP_011529428.1:p.Phe2085Tyr
NM_000132.4:c.6359T>A MANE Select NP_000123.1:p.Phe2120Tyr
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