Canonical Allele Identifier: CA414905538
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903924G>C , CM000685.2:g.154903924G>C GRCh38
NC_000023.10:g.154132199G>C , CM000685.1:g.154132199G>C GRCh37
NC_000023.9:g.153785393G>C NCBI36
NG_011403.1:g.123800C>G
NG_011403.2:g.123800C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5980C>G MANE Select ENSP00000353393.4:p.Leu1994Val
ENST00000360256.8:c.5980C>G ENSP00000353393.4:p.Leu1994Val
NM_000132.3:c.5980C>G NP_000123.1:p.Leu1994Val
XM_011531126.1:c.5875C>G XP_011529428.1:p.Leu1959Val
NM_000132.4:c.5980C>G MANE Select NP_000123.1:p.Leu1994Val