Canonical Allele Identifier: CA319841825
Gene: N6AMT1 HGNC NCBI

Linked Data

dbSNP Id: rs776117169
MyVariant Identifiers: chr21:g.30141024T>C (hg19) chr21:g.28768702T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.28768702T>C , CM000683.2:g.28768702T>C GRCh38
NC_000021.8:g.30141024T>C , CM000683.1:g.30141024T>C GRCh37
NC_000021.7:g.29062895T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754830.1:n.934+53203A>G
XR_002958591.1:n.4651+3292A>G
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