Canonical Allele Identifier: CA29045175
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs548936185
gnomAD v3: 1-114714221-C-T
gnomAD v4: 1-114714221-C-T
MyVariant Identifiers: chr1:g.115256842C>T (hg19) chr1:g.114714221C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714221C>T , CM000663.2:g.114714221C>T GRCh38
NC_000001.10:g.115256842C>T , CM000663.1:g.115256842C>T GRCh37
NC_000001.9:g.115058365C>T NCBI36
NG_007572.1:g.7674G>A , LRG_92:g.7674G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-243G>A MANE Select ENSP00000358548.4:n.112-243G>A
ENST00000369535.4:c.112-243G>A ENSP00000358548.4:n.112-243G>A
NM_002524.4:c.112-243G>A NP_002515.1:n.112-243G>A
NM_002524.5:c.112-243G>A MANE Select NP_002515.1:n.112-243G>A
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