Canonical Allele Identifier: CA2068252622

Linked Data

dbSNP Id: rs1953534694

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122176053T>C , CM000674.2:g.122176053T>C GRCh38
NC_000012.11:g.122660600T>C , CM000674.1:g.122660600T>C GRCh37
NC_000012.10:g.121226553T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+8271T>C (LRRC43) ENSP00000438751.1:n.-406+8271T>C
NM_152759.4:c.-406+8271T>C (LRRC43) NP_689972.3:n.-406+8271T>C
XM_011538326.1:c.-65-1816A>G (IL31) XP_011536628.1:n.-65-1816A>G
NM_152759.5:c.-406+8271T>C (LRRC43) NP_689972.3:n.-406+8271T>C