Canonical Allele Identifier: CA16106788
Gene: TMEM182 HGNC NCBI

Linked Data

dbSNP Id: rs12105421

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102959630C>T , CM000664.2:g.102959630C>T GRCh38
NC_000002.11:g.103576088C>T , CM000664.1:g.103576088C>T GRCh37
NC_000002.10:g.102942520C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000640575.2:c.470-6024C>T ENSP00000492657.2:n.470-6024C>T