Canonical Allele Identifier: CA319177685
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs181237365
MyVariant Identifiers: chr21:g.30149174C>G (hg19) chr21:g.28776852C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776852C>G , CM000683.2:g.28776852C>G GRCh38
NC_000021.8:g.30149174C>G , CM000683.1:g.30149174C>G GRCh37
NC_000021.7:g.29071045C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754830.1:n.934+45053G>C
XR_002958591.1:n.4507-4714G>C
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