Canonical Allele Identifier: CA197094498
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs531944876
gnomAD v3: 9-99356880-T-C
gnomAD v4: 9-99356880-T-C
MyVariant Identifiers: chr9:g.102119162T>C (hg19) chr9:g.99356880T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356880T>C , CM000671.2:g.99356880T>C GRCh38
NC_000009.11:g.102119162T>C , CM000671.1:g.102119162T>C GRCh37
NC_000009.10:g.101158983T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1278A>G
NR_102271.1:n.1419-1278A>G
Search 100 bp 5'
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