Canonical Allele Identifier: CA2628140808

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599503G>A , CM000677.2:g.43599503G>A GRCh38
NC_000015.9:g.43891701G>A , CM000677.1:g.43891701G>A GRCh37
NC_000015.8:g.41678993G>A NCBI36
NG_011636.1:g.24298C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.112G>A (CKMT1B)
ENST00000450892.6:c.*169C>T (STRC) ENSP00000401513.2:n.*169C>T
XM_011521277.1:c.*169C>T (STRC) XP_011519579.1:n.*169C>T
XM_011521278.1:c.*169C>T (STRC) XP_011519580.1:n.*169C>T
XM_011521279.1:c.*169C>T (STRC) XP_011519581.1:n.*169C>T