Canonical Allele Identifier: CA414919387
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154221222A>C (hg19) chrX:g.154992947A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154992947A>C , CM000685.2:g.154992947A>C GRCh38
NC_000023.10:g.154221222A>C , CM000685.1:g.154221222A>C GRCh37
NC_000023.9:g.153874416A>C NCBI36
NG_011403.1:g.34777T>G
NG_011403.2:g.34777T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.590T>G MANE Select ENSP00000353393.4:p.Val197Gly
ENST00000647125.1:c.*376T>G ENSP00000496062.1:n.*376T>G
ENST00000360256.8:c.590T>G ENSP00000353393.4:p.Val197Gly
ENST00000423959.5:c.485T>G ENSP00000409446.1:p.Val162Gly
NM_000132.3:c.590T>G NP_000123.1:p.Val197Gly
XM_011531126.1:c.485T>G XP_011529428.1:p.Val162Gly
NM_000132.4:c.590T>G MANE Select NP_000123.1:p.Val197Gly
Search 100 bp 5'
Search 100 bp 3'