Canonical Allele Identifier: CA548616978

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs1331627604
• gnomAD v2: 3-185686595-C-T
• gnomAD v3: 3-185968806-C-T
• gnomAD v4: 3-185968806-C-T
• MyVariant Identifiers: chr3:g.185686595C>T (hg19) ; chr3:g.185968806C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185968806C>T , CM000665.2:g.185968806C>T	GRCh38
NC_000003.11:g.185686595C>T , CM000665.1:g.185686595C>T	GRCh37
NC_000003.10:g.187169289C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306399.3:n.270+98C>T
ENST00000416764.5:n.349+89C>T
ENST00000422108.5:n.288+157C>T
ENST00000423298.5:n.137-2809C>T
ENST00000436375.5:n.342+98C>T
ENST00000445507.1:n.279+157C>T
NR_033752.2:n.349+89C>T
NR_151491.1:n.137-2809C>T