Canonical Allele Identifier: CA2619795067
Gene: LYZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353336G>T , CM000674.2:g.69353336G>T GRCh38
NC_000012.11:g.69747116G>T , CM000674.1:g.69747116G>T GRCh37
NC_000012.10:g.68033383G>T NCBI36
NG_008195.1:g.9983G>T , LRG_768:g.9983G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*117G>T MANE Select ENSP00000261267.2:n.*117G>T
ENST00000261267.6:c.*117G>T ENSP00000261267.2:n.*117G>T
ENST00000549690.1:c.*71G>T ENSP00000449898.1:n.*71G>T
NM_000239.2:c.*117G>T , LRG_768t1:c.*117G>T NP_000230.1:n.*117G>T
NM_000239.3:c.*117G>T MANE Select NP_000230.1:n.*117G>T