Canonical Allele Identifier: CA633644790
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs1384238232
gnomAD v2: 19-50139468-G-A
MyVariant Identifiers: chr19:g.50139468G>A (hg19) chr19:g.49636211G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636211G>A , CM000681.2:g.49636211G>A GRCh38
NC_000019.9:g.50139468G>A , CM000681.1:g.50139468G>A GRCh37
NC_000019.8:g.54831280G>A NCBI36
NG_042222.1:g.8933C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.454-359C>T MANE Select ENSP00000246792.2:n.454-359C>T
ENST00000246792.3:c.454-359C>T ENSP00000246792.2:n.454-359C>T
ENST00000601532.1:n.594-359C>T
NM_006270.3:c.454-359C>T NP_006261.1:n.454-359C>T
NM_006270.4:c.454-359C>T NP_006261.1:n.454-359C>T
NM_006270.5:c.454-359C>T MANE Select NP_006261.1:n.454-359C>T
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Search 100 bp 3'