Canonical Allele Identifier: CA2173247704

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599496G= , CM000677.2:g.43599496G= GRCh38
NC_000015.9:g.43891694G= , CM000677.1:g.43891694G= GRCh37
NC_000015.8:g.41678986G= NCBI36
NG_011636.1:g.24305C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.105G= (CKMT1B)
ENST00000450892.6:c.*176C= (STRC) ENSP00000401513.2:n.*176C=
XM_011521277.1:c.*176C= (STRC) XP_011519579.1:n.*176C=
XM_011521278.1:c.*176C= (STRC) XP_011519580.1:n.*176C=
XM_011521279.1:c.*176C= (STRC) XP_011519581.1:n.*176C=