Canonical Allele Identifier: CA2173247725

Linked Data

dbSNP Id: rs2085648402

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599549T>C , CM000677.2:g.43599549T>C GRCh38
NC_000015.9:g.43891747T>C , CM000677.1:g.43891747T>C GRCh37
NC_000015.8:g.41679039T>C NCBI36
NG_011636.1:g.24252A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.142+16T>C (CKMT1B)
ENST00000450892.6:c.*123A>G (STRC) ENSP00000401513.2:n.*123A>G
XM_011521277.1:c.*123A>G (STRC) XP_011519579.1:n.*123A>G
XM_011521278.1:c.*123A>G (STRC) XP_011519580.1:n.*123A>G
XM_011521279.1:c.*123A>G (STRC) XP_011519581.1:n.*123A>G