Canonical Allele Identifier: CA474043435

Gene: F2

Linked Data

• dbSNP Id: rs1467246075
• gnomAD v2: 11-46747452-C-T
• gnomAD v4: 11-46725902-C-T
• MyVariant Identifiers: chr11:g.46747452C>T (hg19) ; chr11:g.46725902C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725902C>T , CM000673.2:g.46725902C>T	GRCh38
NC_000011.9:g.46747452C>T , CM000673.1:g.46747452C>T	GRCh37
NC_000011.8:g.46704028C>T	NCBI36
NG_008953.1:g.11710C>T , LRG_551:g.11710C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.603C>T MANE Select	ENSP00000308541.5:p.Gly201=
ENST00000311907.9:c.603C>T	ENSP00000308541.5:p.Gly201=
ENST00000442468.1:c.573C>T	ENSP00000387413.1:p.Gly191=
ENST00000490274.1:n.383C>T
ENST00000530231.5:c.603C>T	ENSP00000433907.1:p.Gly201=
NM_000506.3:c.603C>T	NP_000497.1:p.Gly201=
NM_000506.4:c.603C>T , LRG_551t1:c.603C>T	NP_000497.1:p.Gly201=
NM_001311257.1:c.555C>T	NP_001298186.1:p.Gly185=
XR_428840.2:n.647C>T
XR_428840.4:n.638C>T
NM_000506.5:c.603C>T MANE Select	NP_000497.1:p.Gly201=
NM_001311257.2:c.555C>T	NP_001298186.1:p.Gly185=