Canonical Allele Identifier: CA197094494
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs762734870
gnomAD v3: 9-99356837-G-A
gnomAD v4: 9-99356837-G-A
MyVariant Identifiers: chr9:g.102119119G>A (hg19) chr9:g.99356837G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356837G>A , CM000671.2:g.99356837G>A GRCh38
NC_000009.11:g.102119119G>A , CM000671.1:g.102119119G>A GRCh37
NC_000009.10:g.101158940G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1235C>T
NR_102271.1:n.1419-1235C>T
Search 100 bp 5'
Search 100 bp 3'