Canonical Allele Identifier: CA885828503
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1186008964
gnomAD v4: 1-114709865-G-A
MyVariant Identifiers: chr1:g.115252486G>A (hg19) chr1:g.114709865G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709865G>A , CM000663.2:g.114709865G>A GRCh38
NC_000001.10:g.115252486G>A , CM000663.1:g.115252486G>A GRCh37
NC_000001.9:g.115054009G>A NCBI36
NG_007572.1:g.12030C>T , LRG_92:g.12030C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-137C>T MANE Select ENSP00000358548.4:n.291-137C>T
ENST00000369535.4:c.291-137C>T ENSP00000358548.4:n.291-137C>T
NM_002524.4:c.291-137C>T NP_002515.1:n.291-137C>T
NM_002524.5:c.291-137C>T MANE Select NP_002515.1:n.291-137C>T
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