Canonical Allele Identifier: CA380269289
Gene: F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.46749572C>G (hg19) chr11:g.46728022C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46728022C>G , CM000673.2:g.46728022C>G GRCh38
NC_000011.9:g.46749572C>G , CM000673.1:g.46749572C>G GRCh37
NC_000011.8:g.46706148C>G NCBI36
NG_008953.1:g.13830C>G , LRG_551:g.13830C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.1157C>G MANE Select ENSP00000308541.5:p.Pro386Arg
ENST00000311907.9:c.1157C>G ENSP00000308541.5:p.Pro386Arg
ENST00000530231.5:c.1157C>G ENSP00000433907.1:p.Pro386Arg
NM_000506.3:c.1157C>G NP_000497.1:p.Pro386Arg
NM_000506.4:c.1157C>G , LRG_551t1:c.1157C>G NP_000497.1:p.Pro386Arg
NM_001311257.1:c.1109C>G NP_001298186.1:p.Pro370Arg
XR_428840.2:n.1201C>G
XR_428840.4:n.1192C>G
NM_000506.5:c.1157C>G MANE Select NP_000497.1:p.Pro386Arg
NM_001311257.2:c.1109C>G NP_001298186.1:p.Pro370Arg
Search 100 bp 5'
Search 100 bp 3'