Canonical Allele Identifier: CA385726127
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69744011A>C (hg19) chr12:g.69350231A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69350231A>C , CM000674.2:g.69350231A>C GRCh38
NC_000012.11:g.69744011A>C , CM000674.1:g.69744011A>C GRCh37
NC_000012.10:g.68030278A>C NCBI36
NG_008195.1:g.6878A>C , LRG_768:g.6878A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.260A>C MANE Select ENSP00000261267.2:p.Lys87Thr
ENST00000261267.6:c.260A>C ENSP00000261267.2:p.Lys87Thr
ENST00000548839.1:c.260A>C ENSP00000449969.1:p.Lys87Thr
ENST00000549690.1:c.260A>C ENSP00000449898.1:p.Lys87Thr
NM_000239.2:c.260A>C , LRG_768t1:c.260A>C NP_000230.1:p.Lys87Thr
NM_000239.3:c.260A>C MANE Select NP_000230.1:p.Lys87Thr
Search 100 bp 5'
Search 100 bp 3'