Canonical Allele Identifier: CA385727953
Gene: LYZ HGNC NCBI

Linked Data

gnomAD v4: 12-69353255-T-A
MyVariant Identifiers: chr12:g.69747035T>A (hg19) chr12:g.69353255T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353255T>A , CM000674.2:g.69353255T>A GRCh38
NC_000012.11:g.69747035T>A , CM000674.1:g.69747035T>A GRCh37
NC_000012.10:g.68033302T>A NCBI36
NG_008195.1:g.9902T>A , LRG_768:g.9902T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*36T>A MANE Select ENSP00000261267.2:n.*36T>A
ENST00000261267.6:c.*36T>A ENSP00000261267.2:n.*36T>A
ENST00000549690.1:c.404T>A ENSP00000449898.1:p.Leu135His
NM_000239.2:c.*36T>A , LRG_768t1:c.*36T>A NP_000230.1:n.*36T>A
NM_000239.3:c.*36T>A MANE Select NP_000230.1:n.*36T>A
Search 100 bp 5'
Search 100 bp 3'