Canonical Allele Identifier: CA360289627
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1309870850
gnomAD v2: 5-80502695-C-T
gnomAD v4: 5-81206876-C-T
MyVariant Identifiers: chr5:g.80502695C>T (hg19) chr5:g.81206876C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206876C>T , CM000667.2:g.81206876C>T GRCh38
NC_000005.9:g.80502695C>T , CM000667.1:g.80502695C>T GRCh37
NC_000005.8:g.80538451C>T NCBI36
NG_030334.1:g.251188C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2938C>T MANE Select ENSP00000265080.4:p.His980Tyr
ENST00000265080.8:c.2938C>T ENSP00000265080.4:p.His980Tyr
ENST00000503795.1:c.2938C>T ENSP00000421771.1:p.His980Tyr
NM_006909.2:c.2938C>T NP_008840.1:p.His980Tyr
XM_017009682.2:c.2653C>T XP_016865171.1:p.His885Tyr
XR_002956166.1:n.3054C>T
NM_006909.3:c.2938C>T MANE Select NP_008840.1:p.His980Tyr
Search 100 bp 5'
Search 100 bp 3'