Canonical Allele Identifier: CA445167009
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81206875-C-A
MyVariant Identifiers: chr5:g.80502694C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206875C>A , CM000667.2:g.81206875C>A GRCh38
NC_000005.9:g.80502694C>A , CM000667.1:g.80502694C>A GRCh37
NC_000005.8:g.80538450C>A NCBI36
NG_030334.1:g.251187C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2937C>A MANE Select ENSP00000265080.4:p.Ile979=
ENST00000265080.8:c.2937C>A ENSP00000265080.4:p.Ile979=
ENST00000503795.1:c.2937C>A ENSP00000421771.1:p.Ile979=
NM_006909.2:c.2937C>A NP_008840.1:p.Ile979=
XM_017009682.2:c.2652C>A XP_016865171.1:p.Ile884=
XR_002956166.1:n.3053C>A
NM_006909.3:c.2937C>A MANE Select NP_008840.1:p.Ile979=
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