Canonical Allele Identifier: CA1867363394
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs1830192652

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356853C>T , CM000671.2:g.99356853C>T GRCh38
NC_000009.11:g.102119135C>T , CM000671.1:g.102119135C>T GRCh37
NC_000009.10:g.101158956C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1251G>A
NR_102271.1:n.1419-1251G>A