Canonical Allele Identifier: CA883111728
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs1463400418
gnomAD v3: 19-49636234-A-G
gnomAD v4: 19-49636234-A-G
MyVariant Identifiers: chr19:g.50139491A>G (hg19) chr19:g.49636234A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636234A>G , CM000681.2:g.49636234A>G GRCh38
NC_000019.9:g.50139491A>G , CM000681.1:g.50139491A>G GRCh37
NC_000019.8:g.54831303A>G NCBI36
NG_042222.1:g.8910T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.454-382T>C MANE Select ENSP00000246792.2:n.454-382T>C
ENST00000246792.3:c.454-382T>C ENSP00000246792.2:n.454-382T>C
ENST00000601532.1:n.594-382T>C
NM_006270.3:c.454-382T>C NP_006261.1:n.454-382T>C
NM_006270.4:c.454-382T>C NP_006261.1:n.454-382T>C
NM_006270.5:c.454-382T>C MANE Select NP_006261.1:n.454-382T>C
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