Canonical Allele Identifier: CA341739023
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101738604
MyVariant Identifiers: chr1:g.115252193T>A (hg19) chr1:g.114709572T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709572T>A , CM000663.2:g.114709572T>A GRCh38
NC_000001.10:g.115252193T>A , CM000663.1:g.115252193T>A GRCh37
NC_000001.9:g.115053716T>A NCBI36
NG_007572.1:g.12323A>T , LRG_92:g.12323A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.447A>T MANE Select ENSP00000358548.4:p.Arg149Ser
ENST00000369535.4:c.447A>T ENSP00000358548.4:p.Arg149Ser
NM_002524.4:c.447A>T NP_002515.1:p.Arg149Ser
NM_002524.5:c.447A>T MANE Select NP_002515.1:p.Arg149Ser
Search 100 bp 5'
Search 100 bp 3'