Canonical Allele Identifier: CA2044300777
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1874887178

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353396A>T , CM000674.2:g.69353396A>T GRCh38
NC_000012.11:g.69747176A>T , CM000674.1:g.69747176A>T GRCh37
NC_000012.10:g.68033443A>T NCBI36
NG_008195.1:g.10043A>T , LRG_768:g.10043A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*177A>T MANE Select ENSP00000261267.2:n.*177A>T
ENST00000261267.6:c.*177A>T ENSP00000261267.2:n.*177A>T
ENST00000549690.1:c.*131A>T ENSP00000449898.1:n.*131A>T
NM_000239.2:c.*177A>T , LRG_768t1:c.*177A>T NP_000230.1:n.*177A>T
NM_000239.3:c.*177A>T MANE Select NP_000230.1:n.*177A>T