Canonical Allele Identifier: CA2674453221
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81207107-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207107T>C , CM000667.2:g.81207107T>C GRCh38
NC_000005.9:g.80502926T>C , CM000667.1:g.80502926T>C GRCh37
NC_000005.8:g.80538682T>C NCBI36
NG_030334.1:g.251419T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2968-139T>C MANE Select ENSP00000265080.4:n.2968-139T>C
ENST00000265080.8:c.2968-139T>C ENSP00000265080.4:n.2968-139T>C
ENST00000503795.1:c.2968-139T>C ENSP00000421771.1:n.2968-139T>C
NM_006909.2:c.2968-139T>C NP_008840.1:n.2968-139T>C
XM_017009682.2:c.2683-139T>C XP_016865171.1:n.2683-139T>C
XR_002956166.1:n.3084-139T>C
NM_006909.3:c.2968-139T>C MANE Select NP_008840.1:n.2968-139T>C
Search 100 bp 5'
Search 100 bp 3'