Canonical Allele Identifier: CA445167003
Gene: RASGRF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.80502688T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206869T>C , CM000667.2:g.81206869T>C GRCh38
NC_000005.9:g.80502688T>C , CM000667.1:g.80502688T>C GRCh37
NC_000005.8:g.80538444T>C NCBI36
NG_030334.1:g.251181T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2931T>C MANE Select ENSP00000265080.4:p.Asp977=
ENST00000265080.8:c.2931T>C ENSP00000265080.4:p.Asp977=
ENST00000503795.1:c.2931T>C ENSP00000421771.1:p.Asp977=
NM_006909.2:c.2931T>C NP_008840.1:p.Asp977=
XM_017009682.2:c.2646T>C XP_016865171.1:p.Asp882=
XR_002956166.1:n.3047T>C
NM_006909.3:c.2931T>C MANE Select NP_008840.1:p.Asp977=
Search 100 bp 5'
Search 100 bp 3'