Canonical Allele Identifier: CA2647250235
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114705971-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705971A>T , CM000663.2:g.114705971A>T GRCh38
NC_000001.10:g.115248592A>T , CM000663.1:g.115248592A>T GRCh37
NC_000001.9:g.115050115A>T NCBI36
NG_007572.1:g.15924T>A , LRG_92:g.15924T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2123T>A MANE Select ENSP00000358548.4:n.*2123T>A
ENST00000369535.4:c.*2123T>A ENSP00000358548.4:n.*2123T>A
NM_002524.4:c.*2123T>A NP_002515.1:n.*2123T>A
NM_002524.5:c.*2123T>A MANE Select NP_002515.1:n.*2123T>A
Search 100 bp 5'
Search 100 bp 3'