Canonical Allele Identifier: CA2262224785
Gene: LRRC37A HGNC NCBI

Linked Data

dbSNP Id: rs2458179

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46257341G>C , CM000679.2:g.46257341G>C GRCh38
NC_000017.10:g.44334707G>C , CM000679.1:g.44334707G>C GRCh37
NC_000017.9:g.41690484G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_005257887.3:c.26+9182G>C XP_005257944.1:n.26+9182G>C
XM_011525540.1:c.26+9182G>C XP_011523842.1:n.26+9182G>C