Canonical Allele Identifier: CA1081635057

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs1751797855
• gnomAD v3: 5-132369672-C-T
• gnomAD v4: 5-132369672-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369672C>T , CM000667.2:g.132369672C>T	GRCh38
NC_000005.9:g.131705364C>T , CM000667.1:g.131705364C>T	GRCh37
NC_000005.8:g.131733263C>T	NCBI36
NG_008982.1:g.4964C>T
NG_008982.2:g.4969C>T

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+172G>A