Canonical Allele Identifier: CA1127264269

Gene: NAMA

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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