Canonical Allele Identifier: CA2674453182
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81207016-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207016C>A , CM000667.2:g.81207016C>A GRCh38
NC_000005.9:g.80502835C>A , CM000667.1:g.80502835C>A GRCh37
NC_000005.8:g.80538591C>A NCBI36
NG_030334.1:g.251328C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2967+111C>A MANE Select ENSP00000265080.4:n.2967+111C>A
ENST00000265080.8:c.2967+111C>A ENSP00000265080.4:n.2967+111C>A
ENST00000503795.1:c.2967+111C>A ENSP00000421771.1:n.2967+111C>A
NM_006909.2:c.2967+111C>A NP_008840.1:n.2967+111C>A
XM_017009682.2:c.2682+111C>A XP_016865171.1:n.2682+111C>A
XR_002956166.1:n.3083+111C>A
NM_006909.3:c.2967+111C>A MANE Select NP_008840.1:n.2967+111C>A
Search 100 bp 5'
Search 100 bp 3'