Canonical Allele Identifier: CA480443066
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69747359C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353579C>T , CM000674.2:g.69353579C>T GRCh38
NC_000012.11:g.69747359C>T , CM000674.1:g.69747359C>T GRCh37
NC_000012.10:g.68033626C>T NCBI36
NG_008195.1:g.10226C>T , LRG_768:g.10226C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*360C>T MANE Select ENSP00000261267.2:n.*360C>T
ENST00000261267.6:c.*360C>T ENSP00000261267.2:n.*360C>T
NM_000239.2:c.*360C>T , LRG_768t1:c.*360C>T NP_000230.1:n.*360C>T
NM_000239.3:c.*360C>T MANE Select NP_000230.1:n.*360C>T
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