Canonical Allele Identifier: CA2619795299
Gene: LYZ HGNC NCBI

Linked Data

gnomAD v4: 12-69353481-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353481T>A , CM000674.2:g.69353481T>A GRCh38
NC_000012.11:g.69747261T>A , CM000674.1:g.69747261T>A GRCh37
NC_000012.10:g.68033528T>A NCBI36
NG_008195.1:g.10128T>A , LRG_768:g.10128T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*262T>A MANE Select ENSP00000261267.2:n.*262T>A
ENST00000261267.6:c.*262T>A ENSP00000261267.2:n.*262T>A
ENST00000549690.1:c.*216T>A ENSP00000449898.1:n.*216T>A
NM_000239.2:c.*262T>A , LRG_768t1:c.*262T>A NP_000230.1:n.*262T>A
NM_000239.3:c.*262T>A MANE Select NP_000230.1:n.*262T>A
Search 100 bp 5'
Search 100 bp 3'