Canonical Allele Identifier: CA89843855
Gene: NMRAL2P HGNC NCBI

Linked Data

dbSNP Id: rs888249957
gnomAD v2: 3-185686899-G-C
gnomAD v3: 3-185969110-G-C
gnomAD v4: 3-185969110-G-C
MyVariant Identifiers: chr3:g.185686899G>C (hg19) chr3:g.185969110G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969110G>C , CM000665.2:g.185969110G>C GRCh38
NC_000003.11:g.185686899G>C , CM000665.1:g.185686899G>C GRCh37
NC_000003.10:g.187169593G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+402G>C
ENST00000416764.5:n.349+393G>C
ENST00000422108.5:n.288+461G>C
ENST00000423298.5:n.137-2505G>C
ENST00000436375.5:n.342+402G>C
ENST00000445507.1:n.279+461G>C
NR_033752.2:n.349+393G>C
NR_151491.1:n.137-2505G>C
Search 100 bp 5'
Search 100 bp 3'