Canonical Allele Identifier: CA89843826

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs969747308
• gnomAD v3: 3-185968874-T-C
• gnomAD v4: 3-185968874-T-C
• MyVariant Identifiers: chr3:g.185686663T>C (hg19) ; chr3:g.185968874T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185968874T>C , CM000665.2:g.185968874T>C	GRCh38
NC_000003.11:g.185686663T>C , CM000665.1:g.185686663T>C	GRCh37
NC_000003.10:g.187169357T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306399.3:n.270+166T>C
ENST00000416764.5:n.349+157T>C
ENST00000422108.5:n.288+225T>C
ENST00000423298.5:n.137-2741T>C
ENST00000436375.5:n.342+166T>C
ENST00000445507.1:n.279+225T>C
NR_033752.2:n.349+157T>C
NR_151491.1:n.137-2741T>C