Canonical Allele Identifier: CA360289710
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81206898-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206898T>C , CM000667.2:g.81206898T>C GRCh38
NC_000005.9:g.80502717T>C , CM000667.1:g.80502717T>C GRCh37
NC_000005.8:g.80538473T>C NCBI36
NG_030334.1:g.251210T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2960T>C MANE Select ENSP00000265080.4:p.Ile987Thr
ENST00000265080.8:c.2960T>C ENSP00000265080.4:p.Ile987Thr
ENST00000503795.1:c.2960T>C ENSP00000421771.1:p.Ile987Thr
NM_006909.2:c.2960T>C NP_008840.1:p.Ile987Thr
XM_017009682.2:c.2675T>C XP_016865171.1:p.Ile892Thr
XR_002956166.1:n.3076T>C
NM_006909.3:c.2960T>C MANE Select NP_008840.1:p.Ile987Thr