Canonical Allele Identifier: CA414899907
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154124443G>C (hg19) chrX:g.154896168G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896168G>C , CM000685.2:g.154896168G>C GRCh38
NC_000023.10:g.154124443G>C , CM000685.1:g.154124443G>C GRCh37
NC_000023.9:g.153777637G>C NCBI36
NG_011403.1:g.131556C>G
NG_011403.2:g.131556C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6338C>G MANE Select ENSP00000353393.4:p.Ser2113Cys
ENST00000360256.8:c.6338C>G ENSP00000353393.4:p.Ser2113Cys
NM_000132.3:c.6338C>G NP_000123.1:p.Ser2113Cys
XM_011531126.1:c.6233C>G XP_011529428.1:p.Ser2078Cys
NM_000132.4:c.6338C>G MANE Select NP_000123.1:p.Ser2113Cys
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