Canonical Allele Identifier: CA5967193

Gene: F2

Linked Data

• dbSNP Id: rs781266144
• ExAC: 11:46749514 C / A
• gnomAD v2: 11-46749514-C-A
• gnomAD v3: 11-46727964-C-A
• gnomAD v4: 11-46727964-C-A
• MyVariant Identifiers: chr11:g.46749514C>A (hg19) ; chr11:g.46727964C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727964C>A , CM000673.2:g.46727964C>A	GRCh38
NC_000011.9:g.46749514C>A , CM000673.1:g.46749514C>A	GRCh37
NC_000011.8:g.46706090C>A	NCBI36
NG_008953.1:g.13772C>A , LRG_551:g.13772C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-32C>A MANE Select	ENSP00000308541.5:n.1131-32C>A
ENST00000311907.9:c.1131-32C>A	ENSP00000308541.5:n.1131-32C>A
ENST00000530231.5:c.1131-32C>A	ENSP00000433907.1:n.1131-32C>A
NM_000506.3:c.1131-32C>A	NP_000497.1:n.1131-32C>A
NM_000506.4:c.1131-32C>A , LRG_551t1:c.1131-32C>A	NP_000497.1:n.1131-32C>A
NM_001311257.1:c.1083-32C>A	NP_001298186.1:n.1083-32C>A
XR_428840.2:n.1175-32C>A
XR_428840.4:n.1166-32C>A
NM_000506.5:c.1131-32C>A MANE Select	NP_000497.1:n.1131-32C>A
NM_001311257.2:c.1083-32C>A	NP_001298186.1:n.1083-32C>A