Canonical Allele Identifier: CA414920068
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225340A>C (hg19) chrX:g.154997065A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997065A>C , CM000685.2:g.154997065A>C GRCh38
NC_000023.10:g.154225340A>C , CM000685.1:g.154225340A>C GRCh37
NC_000023.9:g.153878534A>C NCBI36
NG_011403.1:g.30659T>G
NG_011403.2:g.30659T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.296T>G MANE Select ENSP00000353393.4:p.Val99Gly
ENST00000647125.1:c.*82T>G ENSP00000496062.1:n.*82T>G
ENST00000360256.8:c.296T>G ENSP00000353393.4:p.Val99Gly
ENST00000423959.5:c.191T>G ENSP00000409446.1:p.Val64Gly
ENST00000453950.1:c.278T>G ENSP00000389153.1:p.Val93Gly
NM_000132.3:c.296T>G NP_000123.1:p.Val99Gly
XM_011531126.1:c.191T>G XP_011529428.1:p.Val64Gly
NM_000132.4:c.296T>G MANE Select NP_000123.1:p.Val99Gly
Search 100 bp 5'
Search 100 bp 3'