Canonical Allele Identifier: CA120295305

Gene: NT5ELP

Linked Data

• dbSNP Id: rs563092341
• gnomAD v3: 5-64446432-C-T
• gnomAD v4: 5-64446432-C-T
• MyVariant Identifiers: chr5:g.63742259C>T (hg19) ; chr5:g.64446432C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.64446432C>T , CM000667.2:g.64446432C>T	GRCh38
NC_000005.9:g.63742259C>T , CM000667.1:g.63742259C>T	GRCh37
NC_000005.8:g.63778015C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000438016.2:n.222+4239G>A