Canonical Allele Identifier: CA748442660
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1446056332
MyVariant Identifiers: chr21:g.30141057C>T (hg19) chr21:g.28768735C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28768735C>T , CM000683.2:g.28768735C>T GRCh38
NC_000021.8:g.30141057C>T , CM000683.1:g.30141057C>T GRCh37
NC_000021.7:g.29062928C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+53170G>A
XR_002958591.1:n.4651+3259G>A
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