Canonical Allele Identifier: CA319177586
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs991089427
MyVariant Identifiers: chr21:g.30148997G>A (hg19) chr21:g.28776675G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776675G>A , CM000683.2:g.28776675G>A GRCh38
NC_000021.8:g.30148997G>A , CM000683.1:g.30148997G>A GRCh37
NC_000021.7:g.29070868G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45230C>T
XR_002958591.1:n.4507-4537C>T
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