Canonical Allele Identifier: CA1057368979

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs1744963605
• gnomAD v3: 3-185968907-G-A
• gnomAD v4: 3-185968907-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185968907G>A , CM000665.2:g.185968907G>A	GRCh38
NC_000003.11:g.185686696G>A , CM000665.1:g.185686696G>A	GRCh37
NC_000003.10:g.187169390G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+199G>A
ENST00000416764.5:n.349+190G>A
ENST00000422108.5:n.288+258G>A
ENST00000423298.5:n.137-2708G>A
ENST00000436375.5:n.342+199G>A
ENST00000445507.1:n.279+258G>A
NR_033752.2:n.349+190G>A
NR_151491.1:n.137-2708G>A