Canonical Allele Identifier: CA2603461290

Linked Data

dbSNP Id: rs2136020827

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122176241T>C , CM000674.2:g.122176241T>C GRCh38
NC_000012.11:g.122660788T>C , CM000674.1:g.122660788T>C GRCh37
NC_000012.10:g.121226741T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537729.5:c.-405-8278T>C (LRRC43) ENSP00000438751.1:n.-405-8278T>C
NM_152759.4:c.-405-8278T>C (LRRC43) NP_689972.3:n.-405-8278T>C
XM_011538326.1:c.-65-2004A>G (IL31) XP_011536628.1:n.-65-2004A>G
NM_152759.5:c.-405-8278T>C (LRRC43) NP_689972.3:n.-405-8278T>C