Canonical Allele Identifier: CA309505315
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs1038916323
MyVariant Identifiers: chr19:g.50139494T>C (hg19) chr19:g.49636237T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636237T>C , CM000681.2:g.49636237T>C GRCh38
NC_000019.9:g.50139494T>C , CM000681.1:g.50139494T>C GRCh37
NC_000019.8:g.54831306T>C NCBI36
NG_042222.1:g.8907A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+382A>G MANE Select ENSP00000246792.2:n.453+382A>G
ENST00000246792.3:c.453+382A>G ENSP00000246792.2:n.453+382A>G
ENST00000601532.1:n.593+382A>G
NM_006270.3:c.453+382A>G NP_006261.1:n.453+382A>G
NM_006270.4:c.453+382A>G NP_006261.1:n.453+382A>G
NM_006270.5:c.453+382A>G MANE Select NP_006261.1:n.453+382A>G
Search 100 bp 5'
Search 100 bp 3'