Canonical Allele Identifier: CA3329356
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs372723977
ExAC: 5:80502755 A / G
gnomAD v2: 5-80502755-A-G
gnomAD v3: 5-81206936-A-G
gnomAD v4: 5-81206936-A-G
MyVariant Identifiers: chr5:g.80502755A>G (hg19) chr5:g.81206936A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206936A>G , CM000667.2:g.81206936A>G GRCh38
NC_000005.9:g.80502755A>G , CM000667.1:g.80502755A>G GRCh37
NC_000005.8:g.80538511A>G NCBI36
NG_030334.1:g.251248A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2967+31A>G MANE Select ENSP00000265080.4:n.2967+31A>G
ENST00000265080.8:c.2967+31A>G ENSP00000265080.4:n.2967+31A>G
ENST00000503795.1:c.2967+31A>G ENSP00000421771.1:n.2967+31A>G
NM_006909.2:c.2967+31A>G NP_008840.1:n.2967+31A>G
XM_017009682.2:c.2682+31A>G XP_016865171.1:n.2682+31A>G
XR_002956166.1:n.3083+31A>G
NM_006909.3:c.2967+31A>G MANE Select NP_008840.1:n.2967+31A>G
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