Canonical Allele Identifier: CA2578364518
Gene: RASGRF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206997T>A , CM000667.2:g.81206997T>A GRCh38
NC_000005.9:g.80502816T>A , CM000667.1:g.80502816T>A GRCh37
NC_000005.8:g.80538572T>A NCBI36
NG_030334.1:g.251309T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2967+92T>A MANE Select ENSP00000265080.4:n.2967+92T>A
ENST00000265080.8:c.2967+92T>A ENSP00000265080.4:n.2967+92T>A
ENST00000503795.1:c.2967+92T>A ENSP00000421771.1:n.2967+92T>A
NM_006909.2:c.2967+92T>A NP_008840.1:n.2967+92T>A
XM_017009682.2:c.2682+92T>A XP_016865171.1:n.2682+92T>A
XR_002956166.1:n.3083+92T>A
NM_006909.3:c.2967+92T>A MANE Select NP_008840.1:n.2967+92T>A