Canonical Allele Identifier: CA2675194485

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs375038530
• gnomAD v4: 5-132369551-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369551G>C , CM000667.2:g.132369551G>C	GRCh38
NC_000005.9:g.131705243G>C , CM000667.1:g.131705243G>C	GRCh37
NC_000005.8:g.131733142G>C	NCBI36
NG_008982.1:g.4843G>C
NG_008982.2:g.4848G>C

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+293C>G