Canonical Allele Identifier: CA2628140776

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599432G>A , CM000677.2:g.43599432G>A GRCh38
NC_000015.9:g.43891630G>A , CM000677.1:g.43891630G>A GRCh37
NC_000015.8:g.41678922G>A NCBI36
NG_011636.1:g.24369C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.41G>A (CKMT1B)
ENST00000450892.6:c.*240C>T (STRC) ENSP00000401513.2:n.*240C>T
XM_011521277.1:c.*240C>T (STRC) XP_011519579.1:n.*240C>T
XM_011521278.1:c.*240C>T (STRC) XP_011519580.1:n.*240C>T
XM_011521279.1:c.*240C>T (STRC) XP_011519581.1:n.*240C>T