Canonical Allele Identifier: CA1619548181
Community Standard Title: NC_000006.12:g.32408196C>G
Gene: BTNL2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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