Canonical Allele Identifier: CA1558747152
Gene: RASGRF2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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