Canonical Allele Identifier: CA89843818
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs201377901
gnomAD v2: 3-185686640-T-TA
gnomAD v3: 3-185968851-T-TA
gnomAD v4: 3-185968851-T-TA
MyVariant Identifiers: chr3:g.185686640_185686641insA (hg19) chr3:g.185968851_185968852insA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185968857dup , CM000665.2:g.185968857dup GRCh38
NC_000003.11:g.185686646dup , CM000665.1:g.185686646dup GRCh37
NC_000003.10:g.187169340dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+149dup
ENST00000416764.5:n.349+140dup
ENST00000422108.5:n.288+208dup
ENST00000423298.5:n.137-2758dup
ENST00000436375.5:n.342+149dup
ENST00000445507.1:n.279+208dup
NR_033752.2:n.349+140dup
NR_151491.1:n.137-2758dup
Search 100 bp 5'
Search 100 bp 3'