Canonical Allele Identifier: CA414911669
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1309452129
MyVariant Identifiers: chrX:g.154185263T>A (hg19) chrX:g.154956988T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956988T>A , CM000685.2:g.154956988T>A GRCh38
NC_000023.10:g.154185263T>A , CM000685.1:g.154185263T>A GRCh37
NC_000023.9:g.153838457T>A NCBI36
NG_011403.1:g.70736A>T
NG_011403.2:g.70736A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1721A>T MANE Select ENSP00000353393.4:p.Tyr574Phe
ENST00000647125.1:c.*1597A>T ENSP00000496062.1:n.*1597A>T
ENST00000360256.8:c.1721A>T ENSP00000353393.4:p.Tyr574Phe
NM_000132.3:c.1721A>T NP_000123.1:p.Tyr574Phe
XM_011531126.1:c.1616A>T XP_011529428.1:p.Tyr539Phe
NM_000132.4:c.1721A>T MANE Select NP_000123.1:p.Tyr574Phe
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