Canonical Allele Identifier: CA414900354
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154124495C>G (hg19) chrX:g.154896220C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896220C>G , CM000685.2:g.154896220C>G GRCh38
NC_000023.10:g.154124495C>G , CM000685.1:g.154124495C>G GRCh37
NC_000023.9:g.153777689C>G NCBI36
NG_011403.1:g.131504G>C
NG_011403.2:g.131504G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6286G>C MANE Select ENSP00000353393.4:p.Ala2096Pro
ENST00000360256.8:c.6286G>C ENSP00000353393.4:p.Ala2096Pro
NM_000132.3:c.6286G>C NP_000123.1:p.Ala2096Pro
XM_011531126.1:c.6181G>C XP_011529428.1:p.Ala2061Pro
NM_000132.4:c.6286G>C MANE Select NP_000123.1:p.Ala2096Pro
Search 100 bp 5'
Search 100 bp 3'