Canonical Allele Identifier: CA2628140815

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599516A>T , CM000677.2:g.43599516A>T GRCh38
NC_000015.9:g.43891714A>T , CM000677.1:g.43891714A>T GRCh37
NC_000015.8:g.41679006A>T NCBI36
NG_011636.1:g.24285T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.125A>T (CKMT1B)
ENST00000450892.6:c.*156T>A (STRC) ENSP00000401513.2:n.*156T>A
XM_011521277.1:c.*156T>A (STRC) XP_011519579.1:n.*156T>A
XM_011521278.1:c.*156T>A (STRC) XP_011519580.1:n.*156T>A
XM_011521279.1:c.*156T>A (STRC) XP_011519581.1:n.*156T>A