Canonical Allele Identifier: CA380264885

Gene: F2

Linked Data

• dbSNP Id: rs1165489725
• gnomAD v2: 11-46747490-T-C
• gnomAD v4: 11-46725940-T-C
• MyVariant Identifiers: chr11:g.46747490T>C (hg19) ; chr11:g.46725940T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725940T>C , CM000673.2:g.46725940T>C	GRCh38
NC_000011.9:g.46747490T>C , CM000673.1:g.46747490T>C	GRCh37
NC_000011.8:g.46704066T>C	NCBI36
NG_008953.1:g.11748T>C , LRG_551:g.11748T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.641T>C MANE Select	ENSP00000308541.5:p.Val214Ala
ENST00000311907.9:c.641T>C	ENSP00000308541.5:p.Val214Ala
ENST00000442468.1:c.611T>C	ENSP00000387413.1:p.Val204Ala
ENST00000490274.1:n.421T>C
ENST00000530231.5:c.641T>C	ENSP00000433907.1:p.Val214Ala
NM_000506.3:c.641T>C	NP_000497.1:p.Val214Ala
NM_000506.4:c.641T>C , LRG_551t1:c.641T>C	NP_000497.1:p.Val214Ala
NM_001311257.1:c.593T>C	NP_001298186.1:p.Val198Ala
XR_428840.2:n.685T>C
XR_428840.4:n.676T>C
NM_000506.5:c.641T>C MANE Select	NP_000497.1:p.Val214Ala
NM_001311257.2:c.593T>C	NP_001298186.1:p.Val198Ala