Canonical Allele Identifier: CA127195672
Gene: MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs760794767

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132369591C>T , CM000667.2:g.132369591C>T GRCh38
NC_000005.9:g.131705283C>T , CM000667.1:g.131705283C>T GRCh37
NC_000005.8:g.131733182C>T NCBI36
NG_008982.1:g.4883C>T
NG_008982.2:g.4888C>T

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.73+253G>A