Canonical Allele Identifier: CA560478645

Gene: F2R

Linked Data

• gnomAD v2: 5-76023453-T-C
• gnomAD v3: 5-76727628-T-C
• gnomAD v4: 5-76727628-T-C
• MyVariant Identifiers: chr5:g.76023453T>C (hg19) ; chr5:g.76727628T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76727628T>C , CM000667.2:g.76727628T>C	GRCh38
NC_000005.9:g.76023453T>C , CM000667.1:g.76023453T>C	GRCh37
NC_000005.8:g.76059209T>C	NCBI36
NG_032906.1:g.16586T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000319211.5:c.89-4686T>C MANE Select	ENSP00000321326.4:n.89-4686T>C
ENST00000319211.4:c.89-4686T>C	ENSP00000321326.4:n.89-4686T>C
NM_001311313.1:c.-397-1084T>C	NP_001298242.1:n.-397-1084T>C
NM_001992.3:c.89-4686T>C	NP_001983.2:n.89-4686T>C
NM_001992.4:c.89-4686T>C	NP_001983.2:n.89-4686T>C
NM_001992.5:c.89-4686T>C MANE Select	NP_001983.2:n.89-4686T>C
NM_001311313.2:c.-397-1084T>C	NP_001298242.1:n.-397-1084T>C