Canonical Allele Identifier: CA406846037
Gene: RRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.50139910A>C (hg19) chr19:g.49636653A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636653A>C , CM000681.2:g.49636653A>C GRCh38
NC_000019.9:g.50139910A>C , CM000681.1:g.50139910A>C GRCh37
NC_000019.8:g.54831722A>C NCBI36
NG_042222.1:g.8491T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.419T>G MANE Select ENSP00000246792.2:p.Val140Gly
ENST00000246792.3:c.419T>G ENSP00000246792.2:p.Val140Gly
ENST00000601532.1:n.559T>G
NM_006270.3:c.419T>G NP_006261.1:p.Val140Gly
NM_006270.4:c.419T>G NP_006261.1:p.Val140Gly
NM_006270.5:c.419T>G MANE Select NP_006261.1:p.Val140Gly
Search 100 bp 5'
Search 100 bp 3'