Canonical Allele Identifier: CA414904501
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154130329T>G (hg19) chrX:g.154902054T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902054T>G , CM000685.2:g.154902054T>G GRCh38
NC_000023.10:g.154130329T>G , CM000685.1:g.154130329T>G GRCh37
NC_000023.9:g.153783523T>G NCBI36
NG_011403.1:g.125670A>C
NG_011403.2:g.125670A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6112A>C MANE Select ENSP00000353393.4:p.Asn2038His
ENST00000360256.8:c.6112A>C ENSP00000353393.4:p.Asn2038His
NM_000132.3:c.6112A>C NP_000123.1:p.Asn2038His
XM_011531126.1:c.6007A>C XP_011529428.1:p.Asn2003His
NM_000132.4:c.6112A>C MANE Select NP_000123.1:p.Asn2038His
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