Canonical Allele Identifier: CA2044301237
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1874897471

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353648C>T , CM000674.2:g.69353648C>T GRCh38
NC_000012.11:g.69747428C>T , CM000674.1:g.69747428C>T GRCh37
NC_000012.10:g.68033695C>T NCBI36
NG_008195.1:g.10295C>T , LRG_768:g.10295C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*429C>T MANE Select ENSP00000261267.2:n.*429C>T
ENST00000261267.6:c.*429C>T ENSP00000261267.2:n.*429C>T
NM_000239.2:c.*429C>T , LRG_768t1:c.*429C>T NP_000230.1:n.*429C>T
NM_000239.3:c.*429C>T MANE Select NP_000230.1:n.*429C>T