Canonical Allele Identifier: CA480442849
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69747285T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353505T>C , CM000674.2:g.69353505T>C GRCh38
NC_000012.11:g.69747285T>C , CM000674.1:g.69747285T>C GRCh37
NC_000012.10:g.68033552T>C NCBI36
NG_008195.1:g.10152T>C , LRG_768:g.10152T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*286T>C MANE Select ENSP00000261267.2:n.*286T>C
ENST00000261267.6:c.*286T>C ENSP00000261267.2:n.*286T>C
NM_000239.2:c.*286T>C , LRG_768t1:c.*286T>C NP_000230.1:n.*286T>C
NM_000239.3:c.*286T>C MANE Select NP_000230.1:n.*286T>C