Canonical Allele Identifier: CA1619429013
Community Standard Title: NC_000006.12:g.32112369A=

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32112369A= , CM000668.2:g.32112369A= GRCh38
NC_000006.11:g.32080146A= , CM000668.1:g.32080146A= GRCh37
NC_000006.10:g.32188124A= NCBI36
NG_008337.2:g.2006T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442721.1:c.-9+2625T= (TNXB) ENSP00000389946.1:n.-9+2625T=
ENST00000494022.1:n.289+4335T= (ATF6B)