Canonical Allele Identifier: CA803979959
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1459738889
gnomAD v4: 5-132369674-G-C
MyVariant Identifiers: chr5:g.131705366G>C (hg19) chr5:g.132369674G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369674G>C , CM000667.2:g.132369674G>C GRCh38
NC_000005.9:g.131705366G>C , CM000667.1:g.131705366G>C GRCh37
NC_000005.8:g.131733265G>C NCBI36
NG_008982.1:g.4966G>C
NG_008982.2:g.4971G>C

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.73+170C>G
Search 100 bp 5'
Search 100 bp 3'