Canonical Allele Identifier: CA2068252699

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122176141G= , CM000674.2:g.122176141G= GRCh38
NC_000012.11:g.122660688G= , CM000674.1:g.122660688G= GRCh37
NC_000012.10:g.121226641G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537729.5:c.-406+8359G= (LRRC43) ENSP00000438751.1:n.-406+8359G=
NM_152759.4:c.-406+8359G= (LRRC43) NP_689972.3:n.-406+8359G=
XM_011538326.1:c.-65-1904C= (IL31) XP_011536628.1:n.-65-1904C=
NM_152759.5:c.-406+8359G= (LRRC43) NP_689972.3:n.-406+8359G=