Canonical Allele Identifier: CA1127264222

Gene: NAMA

Linked Data

• dbSNP Id: rs1830191452
• gnomAD v3: 9-99356759-G-C
• gnomAD v4: 9-99356759-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356759G>C , CM000671.2:g.99356759G>C	GRCh38
NC_000009.11:g.102119041G>C , CM000671.1:g.102119041G>C	GRCh37
NC_000009.10:g.101158862G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1157C>G
NR_102271.1:n.1419-1157C>G