Canonical Allele Identifier: CA2628140775
Gene: CKMT1B HGNC NCBI
STRC HGNC NCBI

Linked Data

gnomAD v4: 15-43599431-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599431G>T , CM000677.2:g.43599431G>T GRCh38
NC_000015.9:g.43891629G>T , CM000677.1:g.43891629G>T GRCh37
NC_000015.8:g.41678921G>T NCBI36
NG_011636.1:g.24370C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.40G>T (CKMT1B)
ENST00000450892.6:c.*241C>A (STRC) ENSP00000401513.2:n.*241C>A
XM_011521277.1:c.*241C>A (STRC) XP_011519579.1:n.*241C>A
XM_011521278.1:c.*241C>A (STRC) XP_011519580.1:n.*241C>A
XM_011521279.1:c.*241C>A (STRC) XP_011519581.1:n.*241C>A
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