Canonical Allele Identifier: CA244719706

Linked Data

dbSNP Id: rs918989618

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175297G>C , CM000674.2:g.122175297G>C GRCh38
NC_000012.11:g.122659844G>C , CM000674.1:g.122659844G>C GRCh37
NC_000012.10:g.121225797G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537729.5:c.-406+7515G>C (LRRC43) ENSP00000438751.1:n.-406+7515G>C
NM_152759.4:c.-406+7515G>C (LRRC43) NP_689972.3:n.-406+7515G>C
XM_011538326.1:c.-65-1060C>G (IL31) XP_011536628.1:n.-65-1060C>G
NM_152759.5:c.-406+7515G>C (LRRC43) NP_689972.3:n.-406+7515G>C