Canonical Allele Identifier: CA319841830
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs577357843
gnomAD v2: 21-30141065-T-A
gnomAD v3: 21-28768743-T-A
gnomAD v4: 21-28768743-T-A
MyVariant Identifiers: chr21:g.30141065T>A (hg19) chr21:g.28768743T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28768743T>A , CM000683.2:g.28768743T>A GRCh38
NC_000021.8:g.30141065T>A , CM000683.1:g.30141065T>A GRCh37
NC_000021.7:g.29062936T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+53162A>T
XR_002958591.1:n.4651+3251A>T
Search 100 bp 5'
Search 100 bp 3'