Canonical Allele Identifier: CA869139365

Gene: NAMA

Linked Data

• dbSNP Id: rs1270336377
• gnomAD v3: 9-99356779-A-T
• gnomAD v4: 9-99356779-A-T
• MyVariant Identifiers: chr9:g.102119061A>T (hg19) ; chr9:g.99356779A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356779A>T , CM000671.2:g.99356779A>T	GRCh38
NC_000009.11:g.102119061A>T , CM000671.1:g.102119061A>T	GRCh37
NC_000009.10:g.101158882A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1177T>A
NR_102271.1:n.1419-1177T>A