Canonical Allele Identifier: CA903889271

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs927648104
• MyVariant Identifiers: chr3:g.185686694A>T (hg19) ; chr3:g.185968905A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185968905A>T , CM000665.2:g.185968905A>T	GRCh38
NC_000003.11:g.185686694A>T , CM000665.1:g.185686694A>T	GRCh37
NC_000003.10:g.187169388A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306399.3:n.270+197A>T
ENST00000416764.5:n.349+188A>T
ENST00000422108.5:n.288+256A>T
ENST00000423298.5:n.137-2710A>T
ENST00000436375.5:n.342+197A>T
ENST00000445507.1:n.279+256A>T
NR_033752.2:n.349+188A>T
NR_151491.1:n.137-2710A>T