Canonical Allele Identifier: CA1426720844

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs1578505541

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969269T>G , CM000665.2:g.185969269T>G	GRCh38
NC_000003.11:g.185687058T>G , CM000665.1:g.185687058T>G	GRCh37
NC_000003.10:g.187169752T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+561T>G
ENST00000416764.5:n.349+552T>G
ENST00000422108.5:n.288+620T>G
ENST00000423298.5:n.137-2346T>G
ENST00000436375.5:n.342+561T>G
ENST00000445507.1:n.279+620T>G
NR_033752.2:n.349+552T>G
NR_151491.1:n.137-2346T>G