Canonical Allele Identifier: CA414915540
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157191C>T (hg19) chrX:g.154928916C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928916C>T , CM000685.2:g.154928916C>T GRCh38
NC_000023.10:g.154157191C>T , CM000685.1:g.154157191C>T GRCh37
NC_000023.9:g.153810385C>T NCBI36
NG_011403.1:g.98808G>A
NG_011403.2:g.98808G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4874G>A MANE Select ENSP00000353393.4:p.Ser1625Asn
ENST00000360256.8:c.4874G>A ENSP00000353393.4:p.Ser1625Asn
NM_000132.3:c.4874G>A NP_000123.1:p.Ser1625Asn
XM_011531126.1:c.4769G>A XP_011529428.1:p.Ser1590Asn
NM_000132.4:c.4874G>A MANE Select NP_000123.1:p.Ser1625Asn
Search 100 bp 5'
Search 100 bp 3'