Canonical Allele Identifier: CA1426720810

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs1031709659

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969228G>C , CM000665.2:g.185969228G>C	GRCh38
NC_000003.11:g.185687017G>C , CM000665.1:g.185687017G>C	GRCh37
NC_000003.10:g.187169711G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+520G>C
ENST00000416764.5:n.349+511G>C
ENST00000422108.5:n.288+579G>C
ENST00000423298.5:n.137-2387G>C
ENST00000436375.5:n.342+520G>C
ENST00000445507.1:n.279+579G>C
NR_033752.2:n.349+511G>C
NR_151491.1:n.137-2387G>C