Canonical Allele Identifier: CA1078013975
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1312039784
gnomAD v4: 5-81207187-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207187C>T , CM000667.2:g.81207187C>T GRCh38
NC_000005.9:g.80503006C>T , CM000667.1:g.80503006C>T GRCh37
NC_000005.8:g.80538762C>T NCBI36
NG_030334.1:g.251499C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2968-59C>T MANE Select ENSP00000265080.4:n.2968-59C>T
ENST00000265080.8:c.2968-59C>T ENSP00000265080.4:n.2968-59C>T
ENST00000503795.1:c.2968-59C>T ENSP00000421771.1:n.2968-59C>T
NM_006909.2:c.2968-59C>T NP_008840.1:n.2968-59C>T
XM_017009682.2:c.2683-59C>T XP_016865171.1:n.2683-59C>T
XR_002956166.1:n.3084-59C>T
NM_006909.3:c.2968-59C>T MANE Select NP_008840.1:n.2968-59C>T
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