Canonical Allele Identifier: CA445167007
Gene: RASGRF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.80502691C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206872C>T , CM000667.2:g.81206872C>T GRCh38
NC_000005.9:g.80502691C>T , CM000667.1:g.80502691C>T GRCh37
NC_000005.8:g.80538447C>T NCBI36
NG_030334.1:g.251184C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2934C>T MANE Select ENSP00000265080.4:p.Asp978=
ENST00000265080.8:c.2934C>T ENSP00000265080.4:p.Asp978=
ENST00000503795.1:c.2934C>T ENSP00000421771.1:p.Asp978=
NM_006909.2:c.2934C>T NP_008840.1:p.Asp978=
XM_017009682.2:c.2649C>T XP_016865171.1:p.Asp883=
XR_002956166.1:n.3050C>T
NM_006909.3:c.2934C>T MANE Select NP_008840.1:p.Asp978=
Search 100 bp 5'
Search 100 bp 3'