Canonical Allele Identifier: CA414914686
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154928821-G-C
MyVariant Identifiers: chrX:g.154157096G>C (hg19) chrX:g.154928821G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928821G>C , CM000685.2:g.154928821G>C GRCh38
NC_000023.10:g.154157096G>C , CM000685.1:g.154157096G>C GRCh37
NC_000023.9:g.153810290G>C NCBI36
NG_011403.1:g.98903C>G
NG_011403.2:g.98903C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4969C>G MANE Select ENSP00000353393.4:p.Gln1657Glu
ENST00000360256.8:c.4969C>G ENSP00000353393.4:p.Gln1657Glu
NM_000132.3:c.4969C>G NP_000123.1:p.Gln1657Glu
XM_011531126.1:c.4864C>G XP_011529428.1:p.Gln1622Glu
NM_000132.4:c.4969C>G MANE Select NP_000123.1:p.Gln1657Glu
Search 100 bp 5'
Search 100 bp 3'