Canonical Allele Identifier: CA2068252794

Linked Data

dbSNP Id: rs1953536338

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122176275G>A , CM000674.2:g.122176275G>A GRCh38
NC_000012.11:g.122660822G>A , CM000674.1:g.122660822G>A GRCh37
NC_000012.10:g.121226775G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537729.5:c.-405-8244G>A (LRRC43) ENSP00000438751.1:n.-405-8244G>A
NM_152759.4:c.-405-8244G>A (LRRC43) NP_689972.3:n.-405-8244G>A
XM_011538326.1:c.-65-2038C>T (IL31) XP_011536628.1:n.-65-2038C>T
NM_152759.5:c.-405-8244G>A (LRRC43) NP_689972.3:n.-405-8244G>A