Canonical Allele Identifier: CA814488482
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1333905112
MyVariant Identifiers: chr5:g.80502827C>A (hg19) chr5:g.81207008C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207008C>A , CM000667.2:g.81207008C>A GRCh38
NC_000005.9:g.80502827C>A , CM000667.1:g.80502827C>A GRCh37
NC_000005.8:g.80538583C>A NCBI36
NG_030334.1:g.251320C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2967+103C>A MANE Select ENSP00000265080.4:n.2967+103C>A
ENST00000265080.8:c.2967+103C>A ENSP00000265080.4:n.2967+103C>A
ENST00000503795.1:c.2967+103C>A ENSP00000421771.1:n.2967+103C>A
NM_006909.2:c.2967+103C>A NP_008840.1:n.2967+103C>A
XM_017009682.2:c.2682+103C>A XP_016865171.1:n.2682+103C>A
XR_002956166.1:n.3083+103C>A
NM_006909.3:c.2967+103C>A MANE Select NP_008840.1:n.2967+103C>A
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