Canonical Allele Identifier: CA2613334929

Gene: F2

Linked Data

• dbSNP Id: rs2134532319
• gnomAD v4: 11-46726274-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726274T>C , CM000673.2:g.46726274T>C	GRCh38
NC_000011.9:g.46747824T>C , CM000673.1:g.46747824T>C	GRCh37
NC_000011.8:g.46704400T>C	NCBI36
NG_008953.1:g.12082T>C , LRG_551:g.12082T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+101T>C MANE Select	ENSP00000308541.5:n.874+101T>C
ENST00000311907.9:c.874+101T>C	ENSP00000308541.5:n.874+101T>C
ENST00000442468.1:c.844+101T>C	ENSP00000387413.1:n.844+101T>C
ENST00000530231.5:c.874+101T>C	ENSP00000433907.1:n.874+101T>C
NM_000506.3:c.874+101T>C	NP_000497.1:n.874+101T>C
NM_000506.4:c.874+101T>C , LRG_551t1:c.874+101T>C	NP_000497.1:n.874+101T>C
NM_001311257.1:c.826+101T>C	NP_001298186.1:n.826+101T>C
XR_428840.2:n.918+101T>C
XR_428840.4:n.909+101T>C
NM_000506.5:c.874+101T>C MANE Select	NP_000497.1:n.874+101T>C
NM_001311257.2:c.826+101T>C	NP_001298186.1:n.826+101T>C