Canonical Allele Identifier: CA414915111
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1557278308
gnomAD v2: X-154157142-T-C
gnomAD v4: X-154928867-T-C
MyVariant Identifiers: chrX:g.154157142T>C (hg19) chrX:g.154928867T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928867T>C , CM000685.2:g.154928867T>C GRCh38
NC_000023.10:g.154157142T>C , CM000685.1:g.154157142T>C GRCh37
NC_000023.9:g.153810336T>C NCBI36
NG_011403.1:g.98857A>G
NG_011403.2:g.98857A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4923A>G MANE Select ENSP00000353393.4:p.Ile1641Met
ENST00000360256.8:c.4923A>G ENSP00000353393.4:p.Ile1641Met
NM_000132.3:c.4923A>G NP_000123.1:p.Ile1641Met
XM_011531126.1:c.4818A>G XP_011529428.1:p.Ile1606Met
NM_000132.4:c.4923A>G MANE Select NP_000123.1:p.Ile1641Met
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