Canonical Allele Identifier: CA380260354

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46719720A>C , CM000673.2:g.46719720A>C	GRCh38
NC_000011.9:g.46741270A>C , CM000673.1:g.46741270A>C	GRCh37
NC_000011.8:g.46697846A>C	NCBI36
NG_008953.1:g.5528A>C , LRG_551:g.5528A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.98A>C MANE Select	ENSP00000308541.5:p.Gln33Pro
ENST00000311907.9:c.98A>C	ENSP00000308541.5:p.Gln33Pro
ENST00000442468.1:c.68A>C	ENSP00000387413.1:p.Gln23Pro
ENST00000469189.1:n.138A>C
ENST00000530231.5:c.98A>C	ENSP00000433907.1:p.Gln33Pro
NM_000506.3:c.98A>C	NP_000497.1:p.Gln33Pro
NM_000506.4:c.98A>C , LRG_551t1:c.98A>C	NP_000497.1:p.Gln33Pro
NM_001311257.1:c.50A>C	NP_001298186.1:p.Gln17Pro
XR_428840.2:n.142A>C
XR_428840.4:n.133A>C
NM_000506.5:c.98A>C MANE Select	NP_000497.1:p.Gln33Pro
NM_001311257.2:c.50A>C	NP_001298186.1:p.Gln17Pro