Canonical Allele Identifier: CA309505337

Gene: RRAS

Linked Data

• dbSNP Id: rs560036770
• gnomAD v2: 19-50139544-C-G
• gnomAD v3: 19-49636287-C-G
• gnomAD v4: 19-49636287-C-G
• MyVariant Identifiers: chr19:g.50139544C>G (hg19) ; chr19:g.49636287C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636287C>G , CM000681.2:g.49636287C>G	GRCh38
NC_000019.9:g.50139544C>G , CM000681.1:g.50139544C>G	GRCh37
NC_000019.8:g.54831356C>G	NCBI36
NG_042222.1:g.8857G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+332G>C MANE Select	ENSP00000246792.2:n.453+332G>C
ENST00000246792.3:c.453+332G>C	ENSP00000246792.2:n.453+332G>C
ENST00000601532.1:n.593+332G>C
NM_006270.3:c.453+332G>C	NP_006261.1:n.453+332G>C
NM_006270.4:c.453+332G>C	NP_006261.1:n.453+332G>C
NM_006270.5:c.453+332G>C MANE Select	NP_006261.1:n.453+332G>C