Canonical Allele Identifier: CA4481364
Gene: MIR96 HGNC NCBI

Linked Data

dbSNP Id: rs546098287

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.129774713A>G , CM000669.2:g.129774713A>G GRCh38
NC_000007.13:g.129414553A>G , CM000669.1:g.129414553A>G GRCh37
NC_000007.12:g.129201789A>G NCBI36
NG_023385.1:g.5302T>C

Transcript Alleles

HGVS Amino-acid change
NR_029512.1:n.57T>C