Canonical Allele Identifier: CA474043505
Gene: F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.46747464T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725914T>C , CM000673.2:g.46725914T>C GRCh38
NC_000011.9:g.46747464T>C , CM000673.1:g.46747464T>C GRCh37
NC_000011.8:g.46704040T>C NCBI36
NG_008953.1:g.11722T>C , LRG_551:g.11722T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.615T>C MANE Select ENSP00000308541.5:p.Asn205=
ENST00000311907.9:c.615T>C ENSP00000308541.5:p.Asn205=
ENST00000442468.1:c.585T>C ENSP00000387413.1:p.Asn195=
ENST00000490274.1:n.395T>C
ENST00000530231.5:c.615T>C ENSP00000433907.1:p.Asn205=
NM_000506.3:c.615T>C NP_000497.1:p.Asn205=
NM_000506.4:c.615T>C , LRG_551t1:c.615T>C NP_000497.1:p.Asn205=
NM_001311257.1:c.567T>C NP_001298186.1:p.Asn189=
XR_428840.2:n.659T>C
XR_428840.4:n.650T>C
NM_000506.5:c.615T>C MANE Select NP_000497.1:p.Asn205=
NM_001311257.2:c.567T>C NP_001298186.1:p.Asn189=