Canonical Allele Identifier: CA1005996816
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658882845
gnomAD v3: 1-114705222-T-C
gnomAD v4: 1-114705222-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705222T>C , CM000663.2:g.114705222T>C GRCh38
NC_000001.10:g.115247843T>C , CM000663.1:g.115247843T>C GRCh37
NC_000001.9:g.115049366T>C NCBI36
NG_007572.1:g.16673A>G , LRG_92:g.16673A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2872A>G MANE Select ENSP00000358548.4:n.*2872A>G
ENST00000369535.4:c.*2872A>G ENSP00000358548.4:n.*2872A>G
NM_002524.4:c.*2872A>G NP_002515.1:n.*2872A>G
NM_002524.5:c.*2872A>G MANE Select NP_002515.1:n.*2872A>G
Search 100 bp 5'
Search 100 bp 3'