Canonical Allele Identifier: CA360289980
Gene: RASGRF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.80503117C>G (hg19) chr5:g.81207298C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207298C>G , CM000667.2:g.81207298C>G GRCh38
NC_000005.9:g.80503117C>G , CM000667.1:g.80503117C>G GRCh37
NC_000005.8:g.80538873C>G NCBI36
NG_030334.1:g.251610C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.3020C>G MANE Select ENSP00000265080.4:p.Ala1007Gly
ENST00000265080.8:c.3020C>G ENSP00000265080.4:p.Ala1007Gly
ENST00000503795.1:c.3020C>G ENSP00000421771.1:p.Ala1007Gly
NM_006909.2:c.3020C>G NP_008840.1:p.Ala1007Gly
XM_017009682.2:c.2735C>G XP_016865171.1:p.Ala912Gly
XR_002956166.1:n.3136C>G
NM_006909.3:c.3020C>G MANE Select NP_008840.1:p.Ala1007Gly
Search 100 bp 5'
Search 100 bp 3'