Canonical Allele Identifier: CA5967151

Gene: F2

Linked Data

• dbSNP Id: rs768663836
• ExAC: 11:46748258 C / T
• gnomAD v2: 11-46748258-C-T
• gnomAD v3: 11-46726708-C-T
• gnomAD v4: 11-46726708-C-T
• MyVariant Identifiers: chr11:g.46748258C>T (hg19) ; chr11:g.46726708C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726708C>T , CM000673.2:g.46726708C>T	GRCh38
NC_000011.9:g.46748258C>T , CM000673.1:g.46748258C>T	GRCh37
NC_000011.8:g.46704834C>T	NCBI36
NG_008953.1:g.12516C>T , LRG_551:g.12516C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1004-3C>T MANE Select	ENSP00000308541.5:n.1004-3C>T
ENST00000311907.9:c.1004-3C>T	ENSP00000308541.5:n.1004-3C>T
ENST00000530231.5:c.1004-3C>T	ENSP00000433907.1:n.1004-3C>T
NM_000506.3:c.1004-3C>T	NP_000497.1:n.1004-3C>T
NM_000506.4:c.1004-3C>T , LRG_551t1:c.1004-3C>T	NP_000497.1:n.1004-3C>T
NM_001311257.1:c.956-3C>T	NP_001298186.1:n.956-3C>T
XR_428840.2:n.1048-3C>T
XR_428840.4:n.1039-3C>T
NM_000506.5:c.1004-3C>T MANE Select	NP_000497.1:n.1004-3C>T
NM_001311257.2:c.956-3C>T	NP_001298186.1:n.956-3C>T