Canonical Allele Identifier: CA10567739
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs781848666
ExAC: X:154088669 T / TTTTC
gnomAD v2: X-154088669-T-TTTTC
gnomAD v3: X-154860394-T-TTTTC
gnomAD v4: X-154860394-T-TTTTC
MyVariant Identifiers: chrX:g.154088673_154088674insTTTC (hg19) chrX:g.154088669_154088670insTTTC (hg19) chrX:g.154860398_154860399insTTTC (hg38) chrX:g.154860394_154860395insTTTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860411_154860414dup , CM000685.2:g.154860411_154860414dup GRCh38
NC_000023.10:g.154088686_154088689dup , CM000685.1:g.154088686_154088689dup GRCh37
NC_000023.9:g.153741880_153741883dup NCBI36
NG_011403.1:g.167326_167329dup
NG_011403.2:g.167326_167329dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6900+34_6900+37dup MANE Select ENSP00000353393.4:n.6900+34_6900+37dup
ENST00000644698.1:c.633+34_633+37dup ENSP00000495706.1:n.633+34_633+37dup
ENST00000330287.10:c.495+34_495+37dup ENSP00000327895.6:n.495+34_495+37dup
ENST00000360256.8:c.6900+34_6900+37dup ENSP00000353393.4:n.6900+34_6900+37dup
NM_000132.3:c.6900+34_6900+37dup NP_000123.1:n.6900+34_6900+37dup
NM_019863.2:c.495+34_495+37dup NP_063916.1:n.495+34_495+37dup
XM_011531126.1:c.6795+34_6795+37dup XP_011529428.1:n.6795+34_6795+37dup
NM_000132.4:c.6900+34_6900+37dup MANE Select NP_000123.1:n.6900+34_6900+37dup
NM_019863.3:c.495+34_495+37dup NP_063916.1:n.495+34_495+37dup
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