Canonical Allele Identifier: CA89843814

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs924586060
• gnomAD v2: 3-185686579-C-T
• gnomAD v3: 3-185968790-C-T
• gnomAD v4: 3-185968790-C-T
• MyVariant Identifiers: chr3:g.185686579C>T (hg19) ; chr3:g.185968790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185968790C>T , CM000665.2:g.185968790C>T	GRCh38
NC_000003.11:g.185686579C>T , CM000665.1:g.185686579C>T	GRCh37
NC_000003.10:g.187169273C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306399.3:n.270+82C>T
ENST00000416764.5:n.349+73C>T
ENST00000422108.5:n.288+141C>T
ENST00000423298.5:n.137-2825C>T
ENST00000436375.5:n.342+82C>T
ENST00000445507.1:n.279+141C>T
NR_033752.2:n.349+73C>T
NR_151491.1:n.137-2825C>T