Canonical Allele Identifier: CA238507349
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs900978424
gnomAD v3: 12-69353673-A-G
gnomAD v4: 12-69353673-A-G
MyVariant Identifiers: chr12:g.69747453A>G (hg19) chr12:g.69353673A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353673A>G , CM000674.2:g.69353673A>G GRCh38
NC_000012.11:g.69747453A>G , CM000674.1:g.69747453A>G GRCh37
NC_000012.10:g.68033720A>G NCBI36
NG_008195.1:g.10320A>G , LRG_768:g.10320A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*454A>G MANE Select ENSP00000261267.2:n.*454A>G
ENST00000261267.6:c.*454A>G ENSP00000261267.2:n.*454A>G
NM_000239.2:c.*454A>G , LRG_768t1:c.*454A>G NP_000230.1:n.*454A>G
NM_000239.3:c.*454A>G MANE Select NP_000230.1:n.*454A>G
Search 100 bp 5'
Search 100 bp 3'