Canonical Allele Identifier: CA606183990
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1286898522
gnomAD v2: 12-69747067-G-A
gnomAD v4: 12-69353287-G-A
MyVariant Identifiers: chr12:g.69747067G>A (hg19) chr12:g.69353287G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353287G>A , CM000674.2:g.69353287G>A GRCh38
NC_000012.11:g.69747067G>A , CM000674.1:g.69747067G>A GRCh37
NC_000012.10:g.68033334G>A NCBI36
NG_008195.1:g.9934G>A , LRG_768:g.9934G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*68G>A MANE Select ENSP00000261267.2:n.*68G>A
ENST00000261267.6:c.*68G>A ENSP00000261267.2:n.*68G>A
ENST00000549690.1:c.*22G>A ENSP00000449898.1:n.*22G>A
NM_000239.2:c.*68G>A , LRG_768t1:c.*68G>A NP_000230.1:n.*68G>A
NM_000239.3:c.*68G>A MANE Select NP_000230.1:n.*68G>A
Search 100 bp 5'
Search 100 bp 3'