Canonical Allele Identifier: CA238507274
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs551990392
gnomAD v4: 12-69353631-G-A
MyVariant Identifiers: chr12:g.69747411G>A (hg19) chr12:g.69353631G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353631G>A , CM000674.2:g.69353631G>A GRCh38
NC_000012.11:g.69747411G>A , CM000674.1:g.69747411G>A GRCh37
NC_000012.10:g.68033678G>A NCBI36
NG_008195.1:g.10278G>A , LRG_768:g.10278G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*412G>A MANE Select ENSP00000261267.2:n.*412G>A
ENST00000261267.6:c.*412G>A ENSP00000261267.2:n.*412G>A
NM_000239.2:c.*412G>A , LRG_768t1:c.*412G>A NP_000230.1:n.*412G>A
NM_000239.3:c.*412G>A MANE Select NP_000230.1:n.*412G>A
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