Canonical Allele Identifier: CA566378284
Community Standard Title: NC_000006.12:g.32408196C>T
Gene: BTNL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32408196C>T , CM000668.2:g.32408196C>T GRCh38
NC_000006.11:g.32375973C>T , CM000668.1:g.32375973C>T GRCh37
NC_000006.10:g.32483951C>T NCBI36
NG_054759.1:g.5684G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011514755.1:c.-1073G>A XP_011513057.1:n.-1073G>A
XM_011514756.1:c.-1073G>A XP_011513058.1:n.-1073G>A
XM_017011057.1:c.-1073G>A XP_016866546.1:n.-1073G>A