Canonical Allele Identifier: CA952666831

Linked Data

dbSNP Id: rs1953527540

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175288G>T , CM000674.2:g.122175288G>T GRCh38
NC_000012.11:g.122659835G>T , CM000674.1:g.122659835G>T GRCh37
NC_000012.10:g.121225788G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7506G>T (LRRC43) ENSP00000438751.1:n.-406+7506G>T
NM_152759.4:c.-406+7506G>T (LRRC43) NP_689972.3:n.-406+7506G>T
XM_011538326.1:c.-65-1051C>A (IL31) XP_011536628.1:n.-65-1051C>A
NM_152759.5:c.-406+7506G>T (LRRC43) NP_689972.3:n.-406+7506G>T