Canonical Allele Identifier: CA270006951
Gene: CKMT1B HGNC NCBI
STRC HGNC NCBI

Linked Data

dbSNP Id: rs940377059
gnomAD v4: 15-43599562-A-G
MyVariant Identifiers: chr15:g.43891760A>G (hg19) chr15:g.43599562A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599562A>G , CM000677.2:g.43599562A>G GRCh38
NC_000015.9:g.43891760A>G , CM000677.1:g.43891760A>G GRCh37
NC_000015.8:g.41679052A>G NCBI36
NG_011636.1:g.24239T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000411560.1:n.142+29A>G (CKMT1B)
ENST00000450892.6:c.*110T>C (STRC) ENSP00000401513.2:n.*110T>C
XM_011521277.1:c.*110T>C (STRC) XP_011519579.1:n.*110T>C
XM_011521278.1:c.*110T>C (STRC) XP_011519580.1:n.*110T>C
XM_011521279.1:c.*110T>C (STRC) XP_011519581.1:n.*110T>C
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