Canonical Allele Identifier: CA270006910
Gene: CKMT1B HGNC NCBI
STRC HGNC NCBI

Linked Data

dbSNP Id: rs989677480
gnomAD v4: 15-43599408-C-T
MyVariant Identifiers: chr15:g.43891606C>T (hg19) chr15:g.43599408C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599408C>T , CM000677.2:g.43599408C>T GRCh38
NC_000015.9:g.43891606C>T , CM000677.1:g.43891606C>T GRCh37
NC_000015.8:g.41678898C>T NCBI36
NG_011636.1:g.24393G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.17C>T (CKMT1B)
ENST00000450892.6:c.*264G>A (STRC) ENSP00000401513.2:n.*264G>A
XM_011521277.1:c.*264G>A (STRC) XP_011519579.1:n.*264G>A
XM_011521278.1:c.*264G>A (STRC) XP_011519580.1:n.*264G>A
XM_011521279.1:c.*264G>A (STRC) XP_011519581.1:n.*264G>A
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