Canonical Allele Identifier: CA2619794079
Gene: LYZ HGNC NCBI

Linked Data

gnomAD v4: 12-69353627-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353627T>C , CM000674.2:g.69353627T>C GRCh38
NC_000012.11:g.69747407T>C , CM000674.1:g.69747407T>C GRCh37
NC_000012.10:g.68033674T>C NCBI36
NG_008195.1:g.10274T>C , LRG_768:g.10274T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*408T>C MANE Select ENSP00000261267.2:n.*408T>C
ENST00000261267.6:c.*408T>C ENSP00000261267.2:n.*408T>C
NM_000239.2:c.*408T>C , LRG_768t1:c.*408T>C NP_000230.1:n.*408T>C
NM_000239.3:c.*408T>C MANE Select NP_000230.1:n.*408T>C
Search 100 bp 5'
Search 100 bp 3'