Canonical Allele Identifier: CA380264749
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs2064868648

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725904C>T , CM000673.2:g.46725904C>T GRCh38
NC_000011.9:g.46747454C>T , CM000673.1:g.46747454C>T GRCh37
NC_000011.8:g.46704030C>T NCBI36
NG_008953.1:g.11712C>T , LRG_551:g.11712C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.605C>T MANE Select ENSP00000308541.5:p.Ser202Phe
ENST00000311907.9:c.605C>T ENSP00000308541.5:p.Ser202Phe
ENST00000442468.1:c.575C>T ENSP00000387413.1:p.Ser192Phe
ENST00000490274.1:n.385C>T
ENST00000530231.5:c.605C>T ENSP00000433907.1:p.Ser202Phe
NM_000506.3:c.605C>T NP_000497.1:p.Ser202Phe
NM_000506.4:c.605C>T , LRG_551t1:c.605C>T NP_000497.1:p.Ser202Phe
NM_001311257.1:c.557C>T NP_001298186.1:p.Ser186Phe
XR_428840.2:n.649C>T
XR_428840.4:n.640C>T
NM_000506.5:c.605C>T MANE Select NP_000497.1:p.Ser202Phe
NM_001311257.2:c.557C>T NP_001298186.1:p.Ser186Phe