Canonical Allele Identifier: CA406846392
Gene: RRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.50139934C>G (hg19) chr19:g.49636677C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636677C>G , CM000681.2:g.49636677C>G GRCh38
NC_000019.9:g.50139934C>G , CM000681.1:g.50139934C>G GRCh37
NC_000019.8:g.54831746C>G NCBI36
NG_042222.1:g.8467G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.395G>C MANE Select ENSP00000246792.2:p.Arg132Pro
ENST00000246792.3:c.395G>C ENSP00000246792.2:p.Arg132Pro
ENST00000601532.1:n.535G>C
NM_006270.3:c.395G>C NP_006261.1:p.Arg132Pro
NM_006270.4:c.395G>C NP_006261.1:p.Arg132Pro
NM_006270.5:c.395G>C MANE Select NP_006261.1:p.Arg132Pro
Search 100 bp 5'
Search 100 bp 3'