Canonical Allele Identifier: CA2674453246
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81207137-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207137G>T , CM000667.2:g.81207137G>T GRCh38
NC_000005.9:g.80502956G>T , CM000667.1:g.80502956G>T GRCh37
NC_000005.8:g.80538712G>T NCBI36
NG_030334.1:g.251449G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2968-109G>T MANE Select ENSP00000265080.4:n.2968-109G>T
ENST00000265080.8:c.2968-109G>T ENSP00000265080.4:n.2968-109G>T
ENST00000503795.1:c.2968-109G>T ENSP00000421771.1:n.2968-109G>T
NM_006909.2:c.2968-109G>T NP_008840.1:n.2968-109G>T
XM_017009682.2:c.2683-109G>T XP_016865171.1:n.2683-109G>T
XR_002956166.1:n.3084-109G>T
NM_006909.3:c.2968-109G>T MANE Select NP_008840.1:n.2968-109G>T
Search 100 bp 5'
Search 100 bp 3'