Canonical Allele Identifier: CA1867363392
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs1830192618

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356850G>C , CM000671.2:g.99356850G>C GRCh38
NC_000009.11:g.102119132G>C , CM000671.1:g.102119132G>C GRCh37
NC_000009.10:g.101158953G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1248C>G
NR_102271.1:n.1419-1248C>G