Canonical Allele Identifier: CA2173247674

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599424T= , CM000677.2:g.43599424T= GRCh38
NC_000015.9:g.43891622T= , CM000677.1:g.43891622T= GRCh37
NC_000015.8:g.41678914T= NCBI36
NG_011636.1:g.24377A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.33T= (CKMT1B)
ENST00000450892.6:c.*248A= (STRC) ENSP00000401513.2:n.*248A=
XM_011521277.1:c.*248A= (STRC) XP_011519579.1:n.*248A=
XM_011521278.1:c.*248A= (STRC) XP_011519580.1:n.*248A=
XM_011521279.1:c.*248A= (STRC) XP_011519581.1:n.*248A=