Canonical Allele Identifier: CA1867363401
Gene: NAMA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356865C= , CM000671.2:g.99356865C= GRCh38
NC_000009.11:g.102119147C= , CM000671.1:g.102119147C= GRCh37
NC_000009.10:g.101158968C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1263G=
NR_102271.1:n.1419-1263G=