Canonical Allele Identifier: CA49007317
Gene: MIR4432HG HGNC NCBI

Linked Data

dbSNP Id: rs894590481
gnomAD v2: 2-60608803-T-C
gnomAD v3: 2-60381668-T-C
gnomAD v4: 2-60381668-T-C
MyVariant Identifiers: chr2:g.60608803T>C (hg19) chr2:g.60381668T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.60381668T>C , CM000664.2:g.60381668T>C GRCh38
NC_000002.11:g.60608803T>C , CM000664.1:g.60608803T>C GRCh37
NC_000002.10:g.60462307T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_132991.1:n.93+1276A>G
NR_132992.1:n.70+9638A>G
Search 100 bp 5'
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