Canonical Allele Identifier: CA2674453202
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81207047-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207047T>G , CM000667.2:g.81207047T>G GRCh38
NC_000005.9:g.80502866T>G , CM000667.1:g.80502866T>G GRCh37
NC_000005.8:g.80538622T>G NCBI36
NG_030334.1:g.251359T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2967+142T>G MANE Select ENSP00000265080.4:n.2967+142T>G
ENST00000265080.8:c.2967+142T>G ENSP00000265080.4:n.2967+142T>G
ENST00000503795.1:c.2967+142T>G ENSP00000421771.1:n.2967+142T>G
NM_006909.2:c.2967+142T>G NP_008840.1:n.2967+142T>G
XM_017009682.2:c.2682+142T>G XP_016865171.1:n.2682+142T>G
XR_002956166.1:n.3083+142T>G
NM_006909.3:c.2967+142T>G MANE Select NP_008840.1:n.2967+142T>G
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