Canonical Allele Identifier: CA480442916
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs982245735
gnomAD v3: 12-69353528-G-T
gnomAD v4: 12-69353528-G-T
MyVariant Identifiers: chr12:g.69747308G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353528G>T , CM000674.2:g.69353528G>T GRCh38
NC_000012.11:g.69747308G>T , CM000674.1:g.69747308G>T GRCh37
NC_000012.10:g.68033575G>T NCBI36
NG_008195.1:g.10175G>T , LRG_768:g.10175G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*309G>T MANE Select ENSP00000261267.2:n.*309G>T
ENST00000261267.6:c.*309G>T ENSP00000261267.2:n.*309G>T
NM_000239.2:c.*309G>T , LRG_768t1:c.*309G>T NP_000230.1:n.*309G>T
NM_000239.3:c.*309G>T MANE Select NP_000230.1:n.*309G>T
Search 100 bp 5'
Search 100 bp 3'