Canonical Allele Identifier: CA713003450
Gene: CKMT1B HGNC NCBI
STRC HGNC NCBI

Linked Data

dbSNP Id: rs1364892424
gnomAD v4: 15-43599461-G-A
MyVariant Identifiers: chr15:g.43891659G>A (hg19) chr15:g.43599461G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599461G>A , CM000677.2:g.43599461G>A GRCh38
NC_000015.9:g.43891659G>A , CM000677.1:g.43891659G>A GRCh37
NC_000015.8:g.41678951G>A NCBI36
NG_011636.1:g.24340C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.70G>A (CKMT1B)
ENST00000450892.6:c.*211C>T (STRC) ENSP00000401513.2:n.*211C>T
XM_011521277.1:c.*211C>T (STRC) XP_011519579.1:n.*211C>T
XM_011521278.1:c.*211C>T (STRC) XP_011519580.1:n.*211C>T
XM_011521279.1:c.*211C>T (STRC) XP_011519581.1:n.*211C>T
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