Canonical Allele Identifier: CA748443958
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1198136936
MyVariant Identifiers: chr21:g.30149028C>T (hg19) chr21:g.28776706C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776706C>T , CM000683.2:g.28776706C>T GRCh38
NC_000021.8:g.30149028C>T , CM000683.1:g.30149028C>T GRCh37
NC_000021.7:g.29070899C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45199G>A
XR_002958591.1:n.4507-4568G>A
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