Canonical Allele Identifier: CA1020749

Gene: NRAS

Linked Data

• dbSNP Id: rs750670729
• ExAC: 1:115256462 G / A
• gnomAD v2: 1-115256462-G-A
• gnomAD v4: 1-114713841-G-A
• MyVariant Identifiers: chr1:g.115256462G>A (hg19) ; chr1:g.114713841G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713841G>A , CM000663.2:g.114713841G>A	GRCh38
NC_000001.10:g.115256462G>A , CM000663.1:g.115256462G>A	GRCh37
NC_000001.9:g.115057985G>A	NCBI36
NG_007572.1:g.8054C>T , LRG_92:g.8054C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.249C>T MANE Select	ENSP00000358548.4:p.Ala83=
ENST00000369535.4:c.249C>T	ENSP00000358548.4:p.Ala83=
NM_002524.4:c.249C>T	NP_002515.1:p.Ala83=
NM_002524.5:c.249C>T MANE Select	NP_002515.1:p.Ala83=