Canonical Allele Identifier: CA903889398

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs1200116521
• MyVariant Identifiers: chr3:g.185686805G>A (hg19) ; chr3:g.185969016G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969016G>A , CM000665.2:g.185969016G>A	GRCh38
NC_000003.11:g.185686805G>A , CM000665.1:g.185686805G>A	GRCh37
NC_000003.10:g.187169499G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+308G>A
ENST00000416764.5:n.349+299G>A
ENST00000422108.5:n.288+367G>A
ENST00000423298.5:n.137-2599G>A
ENST00000436375.5:n.342+308G>A
ENST00000445507.1:n.279+367G>A
NR_033752.2:n.349+299G>A
NR_151491.1:n.137-2599G>A