Canonical Allele Identifier: CA480442938
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69747316T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353536T>A , CM000674.2:g.69353536T>A GRCh38
NC_000012.11:g.69747316T>A , CM000674.1:g.69747316T>A GRCh37
NC_000012.10:g.68033583T>A NCBI36
NG_008195.1:g.10183T>A , LRG_768:g.10183T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*317T>A MANE Select ENSP00000261267.2:n.*317T>A
ENST00000261267.6:c.*317T>A ENSP00000261267.2:n.*317T>A
NM_000239.2:c.*317T>A , LRG_768t1:c.*317T>A NP_000230.1:n.*317T>A
NM_000239.3:c.*317T>A MANE Select NP_000230.1:n.*317T>A
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