Canonical Allele Identifier: CA536945039
Gene: MMADHC-DT HGNC NCBI
LINC01931 HGNC NCBI

Linked Data

dbSNP Id: rs1424551078
gnomAD v2: 2-150655293-GATT-G
gnomAD v3: 2-149798779-GATT-G
gnomAD v4: 2-149798779-GATT-G
MyVariant Identifiers: chr2:g.150655294_150655296del (hg19) chr2:g.149798780_149798782del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149798783_149798785del , CM000664.2:g.149798783_149798785del GRCh38
NC_000002.11:g.150655297_150655299del , CM000664.1:g.150655297_150655299del GRCh37
NC_000002.10:g.150363543_150363545del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110240.1:n.536-49126_536-49124del (MMADHC-DT)
NR_145421.1:n.1341+5400_1341+5402del (LINC01931)
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