Canonical Allele Identifier: CA1127264253

Gene: NAMA

Linked Data

• dbSNP Id: rs1830192462
• gnomAD v3: 9-99356836-T-A
• gnomAD v4: 9-99356836-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356836T>A , CM000671.2:g.99356836T>A	GRCh38
NC_000009.11:g.102119118T>A , CM000671.1:g.102119118T>A	GRCh37
NC_000009.10:g.101158939T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1234A>T
NR_102271.1:n.1419-1234A>T