Canonical Allele Identifier: CA360289649
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81206883-A-C
MyVariant Identifiers: chr5:g.80502702A>C (hg19) chr5:g.81206883A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206883A>C , CM000667.2:g.81206883A>C GRCh38
NC_000005.9:g.80502702A>C , CM000667.1:g.80502702A>C GRCh37
NC_000005.8:g.80538458A>C NCBI36
NG_030334.1:g.251195A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2945A>C MANE Select ENSP00000265080.4:p.Lys982Thr
ENST00000265080.8:c.2945A>C ENSP00000265080.4:p.Lys982Thr
ENST00000503795.1:c.2945A>C ENSP00000421771.1:p.Lys982Thr
NM_006909.2:c.2945A>C NP_008840.1:p.Lys982Thr
XM_017009682.2:c.2660A>C XP_016865171.1:p.Lys887Thr
XR_002956166.1:n.3061A>C
NM_006909.3:c.2945A>C MANE Select NP_008840.1:p.Lys982Thr
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