Canonical Allele Identifier: CA5967243

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728174G>C , CM000673.2:g.46728174G>C	GRCh38
NC_000011.9:g.46749724G>C , CM000673.1:g.46749724G>C	GRCh37
NC_000011.8:g.46706300G>C	NCBI36
NG_008953.1:g.13982G>C , LRG_551:g.13982G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000506.5:c.1298+11G>C MANE Select	NP_000497.1:n.1298+11G>C
ENST00000311907.10:c.1298+11G>C MANE Select	ENSP00000308541.5:n.1298+11G>C
NM_000506.3:c.1298+11G>C	NP_000497.1:n.1298+11G>C
NM_000506.4:c.1298+11G>C , LRG_551t1:c.1298+11G>C	NP_000497.1:n.1298+11G>C
NM_001311257.1:c.1250+11G>C	NP_001298186.1:n.1250+11G>C
NM_001311257.2:c.1250+11G>C	NP_001298186.1:n.1250+11G>C
ENST00000311907.9:c.1298+11G>C	ENSP00000308541.5:n.1298+11G>C
ENST00000530231.5:c.1298+11G>C	ENSP00000433907.1:n.1298+11G>C
XR_428840.2:n.1342+11G>C
XR_428840.4:n.1333+11G>C