Canonical Allele Identifier: CA2674453085
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81206736-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206736A>T , CM000667.2:g.81206736A>T GRCh38
NC_000005.9:g.80502555A>T , CM000667.1:g.80502555A>T GRCh37
NC_000005.8:g.80538311A>T NCBI36
NG_030334.1:g.251048A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2907-109A>T MANE Select ENSP00000265080.4:n.2907-109A>T
ENST00000265080.8:c.2907-109A>T ENSP00000265080.4:n.2907-109A>T
ENST00000503795.1:c.2907-109A>T ENSP00000421771.1:n.2907-109A>T
NM_006909.2:c.2907-109A>T NP_008840.1:n.2907-109A>T
XM_017009682.2:c.2622-109A>T XP_016865171.1:n.2622-109A>T
XR_002956166.1:n.3023-109A>T
NM_006909.3:c.2907-109A>T MANE Select NP_008840.1:n.2907-109A>T