Canonical Allele Identifier: CA519374747
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154156863T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928588T>C , CM000685.2:g.154928588T>C GRCh38
NC_000023.10:g.154156863T>C , CM000685.1:g.154156863T>C GRCh37
NC_000023.9:g.153810057T>C NCBI36
NG_011403.1:g.99136A>G
NG_011403.2:g.99136A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5202A>G MANE Select ENSP00000353393.4:p.Pro1734=
ENST00000360256.8:c.5202A>G ENSP00000353393.4:p.Pro1734=
NM_000132.3:c.5202A>G NP_000123.1:p.Pro1734=
XM_011531126.1:c.5097A>G XP_011529428.1:p.Pro1699=
NM_000132.4:c.5202A>G MANE Select NP_000123.1:p.Pro1734=
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