Canonical Allele Identifier: CA2768435812
Gene: MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369668A>G , CM000667.2:g.132369668A>G GRCh38
NC_000005.9:g.131705360A>G , CM000667.1:g.131705360A>G GRCh37
NC_000005.8:g.131733259A>G NCBI36
NG_008982.1:g.4960A>G
NG_008982.2:g.4965A>G

Transcript Alleles

HGVS Amino-acid change
NR_110997.1:n.73+176T>C