Canonical Allele Identifier: CA1867363384
Gene: NAMA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356821G= , CM000671.2:g.99356821G= GRCh38
NC_000009.11:g.102119103G= , CM000671.1:g.102119103G= GRCh37
NC_000009.10:g.101158924G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1219C=
NR_102271.1:n.1419-1219C=