Canonical Allele Identifier: CA607946158

Linked Data

dbSNP Id: rs1479085342

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175327G>A , CM000674.2:g.122175327G>A GRCh38
NC_000012.11:g.122659874G>A , CM000674.1:g.122659874G>A GRCh37
NC_000012.10:g.121225827G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7545G>A (LRRC43) ENSP00000438751.1:n.-406+7545G>A
NM_152759.4:c.-406+7545G>A (LRRC43) NP_689972.3:n.-406+7545G>A
XM_011538326.1:c.-65-1090C>T (IL31) XP_011536628.1:n.-65-1090C>T
NM_152759.5:c.-406+7545G>A (LRRC43) NP_689972.3:n.-406+7545G>A