Canonical Allele Identifier: CA885812196
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1488159461
MyVariant Identifiers: chr1:g.115256825G>A (hg19) chr1:g.114714204G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714204G>A , CM000663.2:g.114714204G>A GRCh38
NC_000001.10:g.115256825G>A , CM000663.1:g.115256825G>A GRCh37
NC_000001.9:g.115058348G>A NCBI36
NG_007572.1:g.7691C>T , LRG_92:g.7691C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-226C>T MANE Select ENSP00000358548.4:n.112-226C>T
ENST00000369535.4:c.112-226C>T ENSP00000358548.4:n.112-226C>T
NM_002524.4:c.112-226C>T NP_002515.1:n.112-226C>T
NM_002524.5:c.112-226C>T MANE Select NP_002515.1:n.112-226C>T
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