Canonical Allele Identifier: CA2604424810

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs2126763962
• gnomAD v3: 5-132369668-A-T
• gnomAD v4: 5-132369668-A-T

Genomic Alleles

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

Transcript Alleles

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