Canonical Allele Identifier: CA2628140793

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599450C>T , CM000677.2:g.43599450C>T GRCh38
NC_000015.9:g.43891648C>T , CM000677.1:g.43891648C>T GRCh37
NC_000015.8:g.41678940C>T NCBI36
NG_011636.1:g.24351G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.59C>T (CKMT1B)
ENST00000450892.6:c.*222G>A (STRC) ENSP00000401513.2:n.*222G>A
XM_011521277.1:c.*222G>A (STRC) XP_011519579.1:n.*222G>A
XM_011521278.1:c.*222G>A (STRC) XP_011519580.1:n.*222G>A
XM_011521279.1:c.*222G>A (STRC) XP_011519581.1:n.*222G>A