Canonical Allele Identifier: CA414910223
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154182167T>G (hg19) chrX:g.154953892T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953892T>G , CM000685.2:g.154953892T>G GRCh38
NC_000023.10:g.154182167T>G , CM000685.1:g.154182167T>G GRCh37
NC_000023.9:g.153835361T>G NCBI36
NG_011403.1:g.73832A>C
NG_011403.2:g.73832A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1903A>C MANE Select ENSP00000353393.4:p.Ser635Arg
ENST00000647125.1:c.*1779A>C ENSP00000496062.1:n.*1779A>C
ENST00000360256.8:c.1903A>C ENSP00000353393.4:p.Ser635Arg
NM_000132.3:c.1903A>C NP_000123.1:p.Ser635Arg
XM_011531126.1:c.1798A>C XP_011529428.1:p.Ser600Arg
NM_000132.4:c.1903A>C MANE Select NP_000123.1:p.Ser635Arg
Search 100 bp 5'
Search 100 bp 3'