Canonical Allele Identifier: CA633644796
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs1268113223
gnomAD v2: 19-50139588-T-C
gnomAD v3: 19-49636331-T-C
gnomAD v4: 19-49636331-T-C
MyVariant Identifiers: chr19:g.50139588T>C (hg19) chr19:g.49636331T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636331T>C , CM000681.2:g.49636331T>C GRCh38
NC_000019.9:g.50139588T>C , CM000681.1:g.50139588T>C GRCh37
NC_000019.8:g.54831400T>C NCBI36
NG_042222.1:g.8813A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+288A>G MANE Select ENSP00000246792.2:n.453+288A>G
ENST00000246792.3:c.453+288A>G ENSP00000246792.2:n.453+288A>G
ENST00000601532.1:n.593+288A>G
NM_006270.3:c.453+288A>G NP_006261.1:n.453+288A>G
NM_006270.4:c.453+288A>G NP_006261.1:n.453+288A>G
NM_006270.5:c.453+288A>G MANE Select NP_006261.1:n.453+288A>G
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