Canonical Allele Identifier: CA414904463
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154130327A>C (hg19) chrX:g.154902052A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902052A>C , CM000685.2:g.154902052A>C GRCh38
NC_000023.10:g.154130327A>C , CM000685.1:g.154130327A>C GRCh37
NC_000023.9:g.153783521A>C NCBI36
NG_011403.1:g.125672T>G
NG_011403.2:g.125672T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6114T>G MANE Select ENSP00000353393.4:p.Asn2038Lys
ENST00000360256.8:c.6114T>G ENSP00000353393.4:p.Asn2038Lys
NM_000132.3:c.6114T>G NP_000123.1:p.Asn2038Lys
XM_011531126.1:c.6009T>G XP_011529428.1:p.Asn2003Lys
NM_000132.4:c.6114T>G MANE Select NP_000123.1:p.Asn2038Lys
Search 100 bp 5'
Search 100 bp 3'