Canonical Allele Identifier: CA658233132
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1343833170
COSMIC: COSN15161586
MyVariant Identifiers: chr21:g.30149034C>A (hg19) chr21:g.28776712C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776712C>A , CM000683.2:g.28776712C>A GRCh38
NC_000021.8:g.30149034C>A , CM000683.1:g.30149034C>A GRCh37
NC_000021.7:g.29070905C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45193G>T
XR_002958591.1:n.4507-4574G>T
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