Canonical Allele Identifier: CA5967203
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs767103483

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46728018A>T , CM000673.2:g.46728018A>T GRCh38
NC_000011.9:g.46749568A>T , CM000673.1:g.46749568A>T GRCh37
NC_000011.8:g.46706144A>T NCBI36
NG_008953.1:g.13826A>T , LRG_551:g.13826A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.1153A>T MANE Select ENSP00000308541.5:p.Ser385Cys
ENST00000311907.9:c.1153A>T ENSP00000308541.5:p.Ser385Cys
ENST00000530231.5:c.1153A>T ENSP00000433907.1:p.Ser385Cys
NM_000506.3:c.1153A>T NP_000497.1:p.Ser385Cys
NM_000506.4:c.1153A>T , LRG_551t1:c.1153A>T NP_000497.1:p.Ser385Cys
NM_001311257.1:c.1105A>T NP_001298186.1:p.Ser369Cys
XR_428840.2:n.1197A>T
XR_428840.4:n.1188A>T
NM_000506.5:c.1153A>T MANE Select NP_000497.1:p.Ser385Cys
NM_001311257.2:c.1105A>T NP_001298186.1:p.Ser369Cys