Canonical Allele Identifier: CA1558747218
Gene: RASGRF2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207066G= , CM000667.2:g.81207066G= GRCh38
NC_000005.9:g.80502885G= , CM000667.1:g.80502885G= GRCh37
NC_000005.8:g.80538641G= NCBI36
NG_030334.1:g.251378G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2967+161G= MANE Select ENSP00000265080.4:n.2967+161G=
ENST00000265080.8:c.2967+161G= ENSP00000265080.4:n.2967+161G=
ENST00000503795.1:c.2967+161G= ENSP00000421771.1:n.2967+161G=
NM_006909.2:c.2967+161G= NP_008840.1:n.2967+161G=
XM_017009682.2:c.2682+161G= XP_016865171.1:n.2682+161G=
XR_002956166.1:n.3083+161G=
NM_006909.3:c.2967+161G= MANE Select NP_008840.1:n.2967+161G=
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