Canonical Allele Identifier: CA15406775
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs17228156
gnomAD v2: 5-80502903-T-C
gnomAD v3: 5-81207084-T-C
gnomAD v4: 5-81207084-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207084T>C , CM000667.2:g.81207084T>C GRCh38
NC_000005.9:g.80502903T>C , CM000667.1:g.80502903T>C GRCh37
NC_000005.8:g.80538659T>C NCBI36
NG_030334.1:g.251396T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2968-162T>C MANE Select ENSP00000265080.4:n.2968-162T>C
ENST00000265080.8:c.2968-162T>C ENSP00000265080.4:n.2968-162T>C
ENST00000503795.1:c.2968-162T>C ENSP00000421771.1:n.2968-162T>C
NM_006909.2:c.2968-162T>C NP_008840.1:n.2968-162T>C
XM_017009682.2:c.2683-162T>C XP_016865171.1:n.2683-162T>C
XR_002956166.1:n.3084-162T>C
NM_006909.3:c.2968-162T>C MANE Select NP_008840.1:n.2968-162T>C