Canonical Allele Identifier: CA2628140771

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599426A>C , CM000677.2:g.43599426A>C GRCh38
NC_000015.9:g.43891624A>C , CM000677.1:g.43891624A>C GRCh37
NC_000015.8:g.41678916A>C NCBI36
NG_011636.1:g.24375T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.35A>C (CKMT1B)
ENST00000450892.6:c.*246T>G (STRC) ENSP00000401513.2:n.*246T>G
XM_011521277.1:c.*246T>G (STRC) XP_011519579.1:n.*246T>G
XM_011521278.1:c.*246T>G (STRC) XP_011519580.1:n.*246T>G
XM_011521279.1:c.*246T>G (STRC) XP_011519581.1:n.*246T>G