Canonical Allele Identifier: CA414904540
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154130335A>C (hg19) chrX:g.154902060A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902060A>C , CM000685.2:g.154902060A>C GRCh38
NC_000023.10:g.154130335A>C , CM000685.1:g.154130335A>C GRCh37
NC_000023.9:g.153783529A>C NCBI36
NG_011403.1:g.125664T>G
NG_011403.2:g.125664T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6106T>G MANE Select ENSP00000353393.4:p.Tyr2036Asp
ENST00000360256.8:c.6106T>G ENSP00000353393.4:p.Tyr2036Asp
NM_000132.3:c.6106T>G NP_000123.1:p.Tyr2036Asp
XM_011531126.1:c.6001T>G XP_011529428.1:p.Tyr2001Asp
NM_000132.4:c.6106T>G MANE Select NP_000123.1:p.Tyr2036Asp
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