Canonical Allele Identifier: CA1020767

Gene: NRAS

Linked Data

• dbSNP Id: rs766613733
• ExAC: 1:115256636 G / A
• gnomAD v2: 1-115256636-G-A
• gnomAD v3: 1-114714015-G-A
• gnomAD v4: 1-114714015-G-A
• MyVariant Identifiers: chr1:g.115256636G>A (hg19) ; chr1:g.114714015G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114714015G>A , CM000663.2:g.114714015G>A	GRCh38
NC_000001.10:g.115256636G>A , CM000663.1:g.115256636G>A	GRCh37
NC_000001.9:g.115058159G>A	NCBI36
NG_007572.1:g.7880C>T , LRG_92:g.7880C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.112-37C>T MANE Select	ENSP00000358548.4:n.112-37C>T
ENST00000369535.4:c.112-37C>T	ENSP00000358548.4:n.112-37C>T
NM_002524.4:c.112-37C>T	NP_002515.1:n.112-37C>T
NM_002524.5:c.112-37C>T MANE Select	NP_002515.1:n.112-37C>T