Canonical Allele Identifier: CA480443015
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69747342C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353562C>T , CM000674.2:g.69353562C>T GRCh38
NC_000012.11:g.69747342C>T , CM000674.1:g.69747342C>T GRCh37
NC_000012.10:g.68033609C>T NCBI36
NG_008195.1:g.10209C>T , LRG_768:g.10209C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*343C>T MANE Select ENSP00000261267.2:n.*343C>T
ENST00000261267.6:c.*343C>T ENSP00000261267.2:n.*343C>T
NM_000239.2:c.*343C>T , LRG_768t1:c.*343C>T NP_000230.1:n.*343C>T
NM_000239.3:c.*343C>T MANE Select NP_000230.1:n.*343C>T