Canonical Allele Identifier: CA1127264283

Gene: NAMA

Linked Data

• dbSNP Id: rs1830193471
• gnomAD v3: 9-99356875-A-T
• gnomAD v4: 9-99356875-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356875A>T , CM000671.2:g.99356875A>T	GRCh38
NC_000009.11:g.102119157A>T , CM000671.1:g.102119157A>T	GRCh37
NC_000009.10:g.101158978A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1273T>A
NR_102271.1:n.1419-1273T>A