Canonical Allele Identifier: CA1583137301
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1580866353
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369536A>C , CM000667.2:g.132369536A>C GRCh38
NC_000005.9:g.131705228A>C , CM000667.1:g.131705228A>C GRCh37
NC_000005.8:g.131733127A>C NCBI36
NG_008982.1:g.4828A>C
NG_008982.2:g.4833A>C

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+308T>G
Search 100 bp 5'
Search 100 bp 3'