Canonical Allele Identifier: CA599045299

Gene: F2

Linked Data

• dbSNP Id: rs1317691301
• gnomAD v2: 11-46744910-G-C
• gnomAD v4: 11-46723360-G-C
• MyVariant Identifiers: chr11:g.46744910G>C (hg19) ; chr11:g.46723360G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46723360G>C , CM000673.2:g.46723360G>C	GRCh38
NC_000011.9:g.46744910G>C , CM000673.1:g.46744910G>C	GRCh37
NC_000011.8:g.46701486G>C	NCBI36
NG_008953.1:g.9168G>C , LRG_551:g.9168G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.423-22G>C MANE Select	ENSP00000308541.5:n.423-22G>C
ENST00000311907.9:c.423-22G>C	ENSP00000308541.5:n.423-22G>C
ENST00000442468.1:c.393-22G>C	ENSP00000387413.1:n.393-22G>C
ENST00000490274.1:n.181G>C
ENST00000530231.5:c.423-22G>C	ENSP00000433907.1:n.423-22G>C
NM_000506.3:c.423-22G>C	NP_000497.1:n.423-22G>C
NM_000506.4:c.423-22G>C , LRG_551t1:c.423-22G>C	NP_000497.1:n.423-22G>C
NM_001311257.1:c.375-22G>C	NP_001298186.1:n.375-22G>C
XR_428840.2:n.467-22G>C
XR_428840.4:n.458-22G>C
NM_000506.5:c.423-22G>C MANE Select	NP_000497.1:n.423-22G>C
NM_001311257.2:c.375-22G>C	NP_001298186.1:n.375-22G>C