Canonical Allele Identifier: CA414900301
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154124488A>C (hg19) chrX:g.154896213A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896213A>C , CM000685.2:g.154896213A>C GRCh38
NC_000023.10:g.154124488A>C , CM000685.1:g.154124488A>C GRCh37
NC_000023.9:g.153777682A>C NCBI36
NG_011403.1:g.131511T>G
NG_011403.2:g.131511T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6293T>G MANE Select ENSP00000353393.4:p.Met2098Arg
ENST00000360256.8:c.6293T>G ENSP00000353393.4:p.Met2098Arg
NM_000132.3:c.6293T>G NP_000123.1:p.Met2098Arg
XM_011531126.1:c.6188T>G XP_011529428.1:p.Met2063Arg
NM_000132.4:c.6293T>G MANE Select NP_000123.1:p.Met2098Arg
Search 100 bp 5'
Search 100 bp 3'