Canonical Allele Identifier: CA244719955

Linked Data

dbSNP Id: rs956969845

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122176288A>T , CM000674.2:g.122176288A>T GRCh38
NC_000012.11:g.122660835A>T , CM000674.1:g.122660835A>T GRCh37
NC_000012.10:g.121226788A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537729.5:c.-405-8231A>T (LRRC43) ENSP00000438751.1:n.-405-8231A>T
NM_152759.4:c.-405-8231A>T (LRRC43) NP_689972.3:n.-405-8231A>T
XM_011538326.1:c.-65-2051T>A (IL31) XP_011536628.1:n.-65-2051T>A
NM_152759.5:c.-405-8231A>T (LRRC43) NP_689972.3:n.-405-8231A>T