Canonical Allele Identifier: CA12118274
Gene: RASGRF2 HGNC NCBI
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80987308T>C , CM000667.2:g.80987308T>C GRCh38
NC_000005.9:g.80283127T>C , CM000667.1:g.80283127T>C GRCh37
NC_000005.8:g.80318883T>C NCBI36
NG_030334.1:g.31620T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.288+26282T>C MANE Select ENSP00000265080.4:n.288+26282T>C
ENST00000638442.1:c.288+26282T>C ENSP00000491428.1:n.288+26282T>C
ENST00000265080.8:c.288+26282T>C ENSP00000265080.4:n.288+26282T>C
ENST00000503795.1:c.288+26282T>C ENSP00000421771.1:n.288+26282T>C
NM_006909.2:c.288+26282T>C NP_008840.1:n.288+26282T>C
XM_005248565.1:c.288+26282T>C XP_005248622.1:n.288+26282T>C
XM_017009683.1:c.288+26282T>C XP_016865172.1:n.288+26282T>C
XM_024446141.1:c.288+26282T>C XP_024301909.1:n.288+26282T>C
XM_024446142.1:c.288+26282T>C XP_024301910.1:n.288+26282T>C
XR_002956166.1:n.355+26282T>C
NM_006909.3:c.288+26282T>C MANE Select NP_008840.1:n.288+26282T>C