Canonical Allele Identifier: CA2619795199
Gene: LYZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353406T>C , CM000674.2:g.69353406T>C GRCh38
NC_000012.11:g.69747186T>C , CM000674.1:g.69747186T>C GRCh37
NC_000012.10:g.68033453T>C NCBI36
NG_008195.1:g.10053T>C , LRG_768:g.10053T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*187T>C MANE Select ENSP00000261267.2:n.*187T>C
ENST00000261267.6:c.*187T>C ENSP00000261267.2:n.*187T>C
ENST00000549690.1:c.*141T>C ENSP00000449898.1:n.*141T>C
NM_000239.2:c.*187T>C , LRG_768t1:c.*187T>C NP_000230.1:n.*187T>C
NM_000239.3:c.*187T>C MANE Select NP_000230.1:n.*187T>C