Canonical Allele Identifier: CA748443954

Gene: N6AMT1

Linked Data

• dbSNP Id: rs1216439387
• MyVariant Identifiers: chr21:g.30148960del (hg19) ; chr21:g.28776638del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.28776638del , CM000683.2:g.28776638del	GRCh38
NC_000021.8:g.30148960del , CM000683.1:g.30148960del	GRCh37
NC_000021.7:g.29070831del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001754830.1:n.934+45267del
XR_002958591.1:n.4507-4500del