Canonical Allele Identifier: CA2628140763

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599409T>G , CM000677.2:g.43599409T>G GRCh38
NC_000015.9:g.43891607T>G , CM000677.1:g.43891607T>G GRCh37
NC_000015.8:g.41678899T>G NCBI36
NG_011636.1:g.24392A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.18T>G (CKMT1B)
ENST00000450892.6:c.*263A>C (STRC) ENSP00000401513.2:n.*263A>C
XM_011521277.1:c.*263A>C (STRC) XP_011519579.1:n.*263A>C
XM_011521278.1:c.*263A>C (STRC) XP_011519580.1:n.*263A>C
XM_011521279.1:c.*263A>C (STRC) XP_011519581.1:n.*263A>C