Canonical Allele Identifier: CA1127264293

Gene: NAMA

Linked Data

• dbSNP Id: rs1324864419
• gnomAD v3: 9-99356894-C-G
• gnomAD v4: 9-99356894-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99356894C>G , CM000671.2:g.99356894C>G	GRCh38
NC_000009.11:g.102119176C>G , CM000671.1:g.102119176C>G	GRCh37
NC_000009.10:g.101158997C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_102270.1:n.1971-1292G>C
NR_102271.1:n.1419-1292G>C