Canonical Allele Identifier: CA5967042
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs533673060

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46726014A>G , CM000673.2:g.46726014A>G GRCh38
NC_000011.9:g.46747564A>G , CM000673.1:g.46747564A>G GRCh37
NC_000011.8:g.46704140A>G NCBI36
NG_008953.1:g.11822A>G , LRG_551:g.11822A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.715A>G MANE Select ENSP00000308541.5:p.Ser239Gly
ENST00000311907.9:c.715A>G ENSP00000308541.5:p.Ser239Gly
ENST00000442468.1:c.685A>G ENSP00000387413.1:p.Ser229Gly
ENST00000490274.1:n.495A>G
ENST00000530231.5:c.715A>G ENSP00000433907.1:p.Ser239Gly
NM_000506.3:c.715A>G NP_000497.1:p.Ser239Gly
NM_000506.4:c.715A>G , LRG_551t1:c.715A>G NP_000497.1:p.Ser239Gly
NM_001311257.1:c.667A>G NP_001298186.1:p.Ser223Gly
XR_428840.2:n.759A>G
XR_428840.4:n.750A>G
NM_000506.5:c.715A>G MANE Select NP_000497.1:p.Ser239Gly
NM_001311257.2:c.667A>G NP_001298186.1:p.Ser223Gly