Canonical Allele Identifier: CA1558747251
Gene: RASGRF2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207149A= , CM000667.2:g.81207149A= GRCh38
NC_000005.9:g.80502968A= , CM000667.1:g.80502968A= GRCh37
NC_000005.8:g.80538724A= NCBI36
NG_030334.1:g.251461A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2968-97A= MANE Select ENSP00000265080.4:n.2968-97A=
ENST00000265080.8:c.2968-97A= ENSP00000265080.4:n.2968-97A=
ENST00000503795.1:c.2968-97A= ENSP00000421771.1:n.2968-97A=
NM_006909.2:c.2968-97A= NP_008840.1:n.2968-97A=
XM_017009682.2:c.2683-97A= XP_016865171.1:n.2683-97A=
XR_002956166.1:n.3084-97A=
NM_006909.3:c.2968-97A= MANE Select NP_008840.1:n.2968-97A=
Search 100 bp 5'
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