Canonical Allele Identifier: CA414905609
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903935T>G , CM000685.2:g.154903935T>G GRCh38
NC_000023.10:g.154132210T>G , CM000685.1:g.154132210T>G GRCh37
NC_000023.9:g.153785404T>G NCBI36
NG_011403.1:g.123789A>C
NG_011403.2:g.123789A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5969A>C MANE Select ENSP00000353393.4:p.Tyr1990Ser
ENST00000360256.8:c.5969A>C ENSP00000353393.4:p.Tyr1990Ser
NM_000132.3:c.5969A>C NP_000123.1:p.Tyr1990Ser
XM_011531126.1:c.5864A>C XP_011529428.1:p.Tyr1955Ser
NM_000132.4:c.5969A>C MANE Select NP_000123.1:p.Tyr1990Ser