Canonical Allele Identifier: CA2620150229
Gene: LUM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111549C>T , CM000674.2:g.91111549C>T GRCh38
NC_000012.11:g.91505326C>T , CM000674.1:g.91505326C>T GRCh37
NC_000012.10:g.90029457C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-173G>A ENSP00000266718.4:n.-173G>A
NM_002345.3:c.-173G>A NP_002336.1:n.-173G>A