Canonical Allele Identifier: CA606184002
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1565670433
gnomAD v2: 12-69747274-G-GTTTTTTTTTTTTTT
gnomAD v3: 12-69353494-G-GTTTTTTTTTTTTTT
gnomAD v4: 12-69353494-G-GTTTTTTTTTTTTTT
MyVariant Identifiers: chr12:g.69747274_69747275insTTTTTTTTTTTTTT (hg19) chr12:g.69353494_69353495insTTTTTTTTTTTTTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353496_69353497insTTTTTTTTTTTTTT , CM000674.2:g.69353496_69353497insTTTTTTTTTTTTTT GRCh38
NC_000012.11:g.69747276_69747277insTTTTTTTTTTTTTT , CM000674.1:g.69747276_69747277insTTTTTTTTTTTTTT GRCh37
NC_000012.10:g.68033543_68033544insTTTTTTTTTTTTTT NCBI36
NG_008195.1:g.10143_10144insTTTTTTTTTTTTTT , LRG_768:g.10143_10144insTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*277_*278insTTTTTTTTTTTTTT MANE Select ENSP00000261267.2:n.*277_*278insTTTTTTTTTTTTTT
ENST00000261267.6:c.*277_*278insTTTTTTTTTTTTTT ENSP00000261267.2:n.*277_*278insTTTTTTTTTTTTTT
NM_000239.2:c.*277_*278insTTTTTTTTTTTTTT , LRG_768t1:c.*277_*278insTTTTTTTTTTTTTT NP_000230.1:n.*277_*278insTTTTTTTTTTTTTT
NM_000239.3:c.*277_*278insTTTTTTTTTTTTTT MANE Select NP_000230.1:n.*277_*278insTTTTTTTTTTTTTT
Search 100 bp 5'
Search 100 bp 3'