Canonical Allele Identifier: CA360289567
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81206861-G-T
MyVariant Identifiers: chr5:g.80502680G>T (hg19) chr5:g.81206861G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206861G>T , CM000667.2:g.81206861G>T GRCh38
NC_000005.9:g.80502680G>T , CM000667.1:g.80502680G>T GRCh37
NC_000005.8:g.80538436G>T NCBI36
NG_030334.1:g.251173G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2923G>T MANE Select ENSP00000265080.4:p.Asp975Tyr
ENST00000265080.8:c.2923G>T ENSP00000265080.4:p.Asp975Tyr
ENST00000503795.1:c.2923G>T ENSP00000421771.1:p.Asp975Tyr
NM_006909.2:c.2923G>T NP_008840.1:p.Asp975Tyr
XM_017009682.2:c.2638G>T XP_016865171.1:p.Asp880Tyr
XR_002956166.1:n.3039G>T
NM_006909.3:c.2923G>T MANE Select NP_008840.1:p.Asp975Tyr
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