Canonical Allele Identifier: CA2674453167
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81206988-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206988G>T , CM000667.2:g.81206988G>T GRCh38
NC_000005.9:g.80502807G>T , CM000667.1:g.80502807G>T GRCh37
NC_000005.8:g.80538563G>T NCBI36
NG_030334.1:g.251300G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2967+83G>T MANE Select ENSP00000265080.4:n.2967+83G>T
ENST00000265080.8:c.2967+83G>T ENSP00000265080.4:n.2967+83G>T
ENST00000503795.1:c.2967+83G>T ENSP00000421771.1:n.2967+83G>T
NM_006909.2:c.2967+83G>T NP_008840.1:n.2967+83G>T
XM_017009682.2:c.2682+83G>T XP_016865171.1:n.2682+83G>T
XR_002956166.1:n.3083+83G>T
NM_006909.3:c.2967+83G>T MANE Select NP_008840.1:n.2967+83G>T