Canonical Allele Identifier: CA560478646

Gene: F2R

Linked Data

• dbSNP Id: rs1190132248
• gnomAD v2: 5-76023456-T-C
• MyVariant Identifiers: chr5:g.76023456T>C (hg19) ; chr5:g.76727631T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76727631T>C , CM000667.2:g.76727631T>C	GRCh38
NC_000005.9:g.76023456T>C , CM000667.1:g.76023456T>C	GRCh37
NC_000005.8:g.76059212T>C	NCBI36
NG_032906.1:g.16589T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000319211.5:c.89-4683T>C MANE Select	ENSP00000321326.4:n.89-4683T>C
ENST00000319211.4:c.89-4683T>C	ENSP00000321326.4:n.89-4683T>C
NM_001311313.1:c.-397-1081T>C	NP_001298242.1:n.-397-1081T>C
NM_001992.3:c.89-4683T>C	NP_001983.2:n.89-4683T>C
NM_001992.4:c.89-4683T>C	NP_001983.2:n.89-4683T>C
NM_001992.5:c.89-4683T>C MANE Select	NP_001983.2:n.89-4683T>C
NM_001311313.2:c.-397-1081T>C	NP_001298242.1:n.-397-1081T>C