Canonical Allele Identifier: CA2580598016
Gene: NAMA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356808G>C , CM000671.2:g.99356808G>C GRCh38
NC_000009.11:g.102119090G>C , CM000671.1:g.102119090G>C GRCh37
NC_000009.10:g.101158911G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1206C>G
NR_102271.1:n.1419-1206C>G