Canonical Allele Identifier: CA480442985
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69747333A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353553A>C , CM000674.2:g.69353553A>C GRCh38
NC_000012.11:g.69747333A>C , CM000674.1:g.69747333A>C GRCh37
NC_000012.10:g.68033600A>C NCBI36
NG_008195.1:g.10200A>C , LRG_768:g.10200A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*334A>C MANE Select ENSP00000261267.2:n.*334A>C
ENST00000261267.6:c.*334A>C ENSP00000261267.2:n.*334A>C
NM_000239.2:c.*334A>C , LRG_768t1:c.*334A>C NP_000230.1:n.*334A>C
NM_000239.3:c.*334A>C MANE Select NP_000230.1:n.*334A>C
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