Canonical Allele Identifier: CA2173247703

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599491A= , CM000677.2:g.43599491A= GRCh38
NC_000015.9:g.43891689A= , CM000677.1:g.43891689A= GRCh37
NC_000015.8:g.41678981A= NCBI36
NG_011636.1:g.24310T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.100A= (CKMT1B)
ENST00000450892.6:c.*181T= (STRC) ENSP00000401513.2:n.*181T=
XM_011521277.1:c.*181T= (STRC) XP_011519579.1:n.*181T=
XM_011521278.1:c.*181T= (STRC) XP_011519580.1:n.*181T=
XM_011521279.1:c.*181T= (STRC) XP_011519581.1:n.*181T=