Canonical Allele Identifier: CA197094493
Gene: NAMA HGNC NCBI

Linked Data

dbSNP Id: rs562964059
gnomAD v2: 9-102119105-C-A
gnomAD v3: 9-99356823-C-A
gnomAD v4: 9-99356823-C-A
MyVariant Identifiers: chr9:g.102119105C>A (hg19) chr9:g.99356823C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99356823C>A , CM000671.2:g.99356823C>A GRCh38
NC_000009.11:g.102119105C>A , CM000671.1:g.102119105C>A GRCh37
NC_000009.10:g.101158926C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_102270.1:n.1971-1221G>T
NR_102271.1:n.1419-1221G>T
Search 100 bp 5'
Search 100 bp 3'