Canonical Allele Identifier: CA127195657

Gene: MIR3936HG

Linked Data

• dbSNP Id: rs57961304
• gnomAD v4: 5-132369581-C-T
• MyVariant Identifiers: chr5:g.131705273C>T (hg19) ; chr5:g.132369581C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369581C>T , CM000667.2:g.132369581C>T	GRCh38
NC_000005.9:g.131705273C>T , CM000667.1:g.131705273C>T	GRCh37
NC_000005.8:g.131733172C>T	NCBI36
NG_008982.1:g.4873C>T
NG_008982.2:g.4878C>T

Transcript Alleles

HGVS	Amino-acid Change
NR_110997.1:n.73+263G>A