Canonical Allele Identifier: CA560571137
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1175560957
gnomAD v2: 5-80502642-G-T
gnomAD v4: 5-81206823-G-T
COSMIC: COSN5851868
MyVariant Identifiers: chr5:g.80502642G>T (hg19) chr5:g.81206823G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206823G>T , CM000667.2:g.81206823G>T GRCh38
NC_000005.9:g.80502642G>T , CM000667.1:g.80502642G>T GRCh37
NC_000005.8:g.80538398G>T NCBI36
NG_030334.1:g.251135G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2907-22G>T MANE Select ENSP00000265080.4:n.2907-22G>T
ENST00000265080.8:c.2907-22G>T ENSP00000265080.4:n.2907-22G>T
ENST00000503795.1:c.2907-22G>T ENSP00000421771.1:n.2907-22G>T
NM_006909.2:c.2907-22G>T NP_008840.1:n.2907-22G>T
XM_017009682.2:c.2622-22G>T XP_016865171.1:n.2622-22G>T
XR_002956166.1:n.3023-22G>T
NM_006909.3:c.2907-22G>T MANE Select NP_008840.1:n.2907-22G>T
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