Canonical Allele Identifier: CA2504751466
Gene: NAMA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356841C>A , CM000671.2:g.99356841C>A GRCh38
NC_000009.11:g.102119123C>A , CM000671.1:g.102119123C>A GRCh37
NC_000009.10:g.101158944C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1239G>T
NR_102271.1:n.1419-1239G>T