Canonical Allele Identifier: CA637182976
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs1370428553
gnomAD v2: 21-30149079-G-A
gnomAD v3: 21-28776757-G-A
gnomAD v4: 21-28776757-G-A
MyVariant Identifiers: chr21:g.30149079G>A (hg19) chr21:g.28776757G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28776757G>A , CM000683.2:g.28776757G>A GRCh38
NC_000021.8:g.30149079G>A , CM000683.1:g.30149079G>A GRCh37
NC_000021.7:g.29070950G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+45148C>T
XR_002958591.1:n.4507-4619C>T
Search 100 bp 5'
Search 100 bp 3'