Canonical Allele Identifier: CA2668921126

Gene: NMRAL2P

Linked Data

• gnomAD v4: 3-185968794-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185968794A>C , CM000665.2:g.185968794A>C	GRCh38
NC_000003.11:g.185686583A>C , CM000665.1:g.185686583A>C	GRCh37
NC_000003.10:g.187169277A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+86A>C
ENST00000416764.5:n.349+77A>C
ENST00000422108.5:n.288+145A>C
ENST00000423298.5:n.137-2821A>C
ENST00000436375.5:n.342+86A>C
ENST00000445507.1:n.279+145A>C
NR_033752.2:n.349+77A>C
NR_151491.1:n.137-2821A>C