Canonical Allele Identifier: CA414915448
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157180T>C (hg19) chrX:g.154928905T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928905T>C , CM000685.2:g.154928905T>C GRCh38
NC_000023.10:g.154157180T>C , CM000685.1:g.154157180T>C GRCh37
NC_000023.9:g.153810374T>C NCBI36
NG_011403.1:g.98819A>G
NG_011403.2:g.98819A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4885A>G MANE Select ENSP00000353393.4:p.Ile1629Val
ENST00000360256.8:c.4885A>G ENSP00000353393.4:p.Ile1629Val
NM_000132.3:c.4885A>G NP_000123.1:p.Ile1629Val
XM_011531126.1:c.4780A>G XP_011529428.1:p.Ile1594Val
NM_000132.4:c.4885A>G MANE Select NP_000123.1:p.Ile1629Val
Search 100 bp 5'
Search 100 bp 3'