Canonical Allele Identifier: CA309505322
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs905379157
gnomAD v2: 19-50139512-C-T
gnomAD v3: 19-49636255-C-T
gnomAD v4: 19-49636255-C-T
MyVariant Identifiers: chr19:g.50139512C>T (hg19) chr19:g.49636255C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636255C>T , CM000681.2:g.49636255C>T GRCh38
NC_000019.9:g.50139512C>T , CM000681.1:g.50139512C>T GRCh37
NC_000019.8:g.54831324C>T NCBI36
NG_042222.1:g.8889G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+364G>A MANE Select ENSP00000246792.2:n.453+364G>A
ENST00000246792.3:c.453+364G>A ENSP00000246792.2:n.453+364G>A
ENST00000601532.1:n.593+364G>A
NM_006270.3:c.453+364G>A NP_006261.1:n.453+364G>A
NM_006270.4:c.453+364G>A NP_006261.1:n.453+364G>A
NM_006270.5:c.453+364G>A MANE Select NP_006261.1:n.453+364G>A
Search 100 bp 5'
Search 100 bp 3'