Canonical Allele Identifier: CA238507320
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs566937585
gnomAD v3: 12-69353655-AT-A
gnomAD v4: 12-69353655-AT-A
MyVariant Identifiers: chr12:g.69747436del (hg19) chr12:g.69353656del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353661del , CM000674.2:g.69353661del GRCh38
NC_000012.11:g.69747441del , CM000674.1:g.69747441del GRCh37
NC_000012.10:g.68033708del NCBI36
NG_008195.1:g.10308del , LRG_768:g.10308del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*442del MANE Select ENSP00000261267.2:n.*442del
ENST00000261267.6:c.*442del ENSP00000261267.2:n.*442del
NM_000239.2:c.*442del , LRG_768t1:c.*442del NP_000230.1:n.*442del
NM_000239.3:c.*442del MANE Select NP_000230.1:n.*442del
Search 100 bp 5'
Search 100 bp 3'