Canonical Allele Identifier: CA1275502563
Gene: TMEM182 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102959700C= , CM000664.2:g.102959700C= GRCh38
NC_000002.11:g.103576158C= , CM000664.1:g.103576158C= GRCh37
NC_000002.10:g.102942590C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000640575.2:c.470-5954C= ENSP00000492657.2:n.470-5954C=