Canonical Allele Identifier: CA414906065
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132274T>G (hg19) chrX:g.154903999T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903999T>G , CM000685.2:g.154903999T>G GRCh38
NC_000023.10:g.154132274T>G , CM000685.1:g.154132274T>G GRCh37
NC_000023.9:g.153785468T>G NCBI36
NG_011403.1:g.123725A>C
NG_011403.2:g.123725A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5905A>C MANE Select ENSP00000353393.4:p.Asn1969His
ENST00000360256.8:c.5905A>C ENSP00000353393.4:p.Asn1969His
NM_000132.3:c.5905A>C NP_000123.1:p.Asn1969His
XM_011531126.1:c.5800A>C XP_011529428.1:p.Asn1934His
NM_000132.4:c.5905A>C MANE Select NP_000123.1:p.Asn1969His
Search 100 bp 5'
Search 100 bp 3'