Canonical Allele Identifier: CA480443119
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69747378C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353598C>G , CM000674.2:g.69353598C>G GRCh38
NC_000012.11:g.69747378C>G , CM000674.1:g.69747378C>G GRCh37
NC_000012.10:g.68033645C>G NCBI36
NG_008195.1:g.10245C>G , LRG_768:g.10245C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*379C>G MANE Select ENSP00000261267.2:n.*379C>G
ENST00000261267.6:c.*379C>G ENSP00000261267.2:n.*379C>G
NM_000239.2:c.*379C>G , LRG_768t1:c.*379C>G NP_000230.1:n.*379C>G
NM_000239.3:c.*379C>G MANE Select NP_000230.1:n.*379C>G
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