Canonical Allele Identifier: CA684581639

Linked Data

dbSNP Id: rs1171329844

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122176115A>G , CM000674.2:g.122176115A>G GRCh38
NC_000012.11:g.122660662A>G , CM000674.1:g.122660662A>G GRCh37
NC_000012.10:g.121226615A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537729.5:c.-406+8333A>G (LRRC43) ENSP00000438751.1:n.-406+8333A>G
NM_152759.4:c.-406+8333A>G (LRRC43) NP_689972.3:n.-406+8333A>G
XM_011538326.1:c.-65-1878T>C (IL31) XP_011536628.1:n.-65-1878T>C
NM_152759.5:c.-406+8333A>G (LRRC43) NP_689972.3:n.-406+8333A>G