Canonical Allele Identifier: CA360289553
Gene: RASGRF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.80502676A>T (hg19) chr5:g.81206857A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206857A>T , CM000667.2:g.81206857A>T GRCh38
NC_000005.9:g.80502676A>T , CM000667.1:g.80502676A>T GRCh37
NC_000005.8:g.80538432A>T NCBI36
NG_030334.1:g.251169A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2919A>T MANE Select ENSP00000265080.4:p.Gln973His
ENST00000265080.8:c.2919A>T ENSP00000265080.4:p.Gln973His
ENST00000503795.1:c.2919A>T ENSP00000421771.1:p.Gln973His
NM_006909.2:c.2919A>T NP_008840.1:p.Gln973His
XM_017009682.2:c.2634A>T XP_016865171.1:p.Gln878His
XR_002956166.1:n.3035A>T
NM_006909.3:c.2919A>T MANE Select NP_008840.1:p.Gln973His
Search 100 bp 5'
Search 100 bp 3'