Canonical Allele Identifier: CA748443964
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1400186019
MyVariant Identifiers: chr21:g.30149137A>C (hg19) chr21:g.28776815A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776815A>C , CM000683.2:g.28776815A>C GRCh38
NC_000021.8:g.30149137A>C , CM000683.1:g.30149137A>C GRCh37
NC_000021.7:g.29071008A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45090T>G
XR_002958591.1:n.4507-4677T>G
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