Canonical Allele Identifier: CA607946153

Linked Data

dbSNP Id: rs1310377584

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122175265G>C , CM000674.2:g.122175265G>C GRCh38
NC_000012.11:g.122659812G>C , CM000674.1:g.122659812G>C GRCh37
NC_000012.10:g.121225765G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537729.5:c.-406+7483G>C (LRRC43) ENSP00000438751.1:n.-406+7483G>C
NM_152759.4:c.-406+7483G>C (LRRC43) NP_689972.3:n.-406+7483G>C
XM_011538326.1:c.-65-1028C>G (IL31) XP_011536628.1:n.-65-1028C>G
NM_152759.5:c.-406+7483G>C (LRRC43) NP_689972.3:n.-406+7483G>C