Canonical Allele Identifier: CA480442895
Gene: LYZ HGNC NCBI

Linked Data

gnomAD v4: 12-69353521-C-G
MyVariant Identifiers: chr12:g.69747301C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353521C>G , CM000674.2:g.69353521C>G GRCh38
NC_000012.11:g.69747301C>G , CM000674.1:g.69747301C>G GRCh37
NC_000012.10:g.68033568C>G NCBI36
NG_008195.1:g.10168C>G , LRG_768:g.10168C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*302C>G MANE Select ENSP00000261267.2:n.*302C>G
ENST00000261267.6:c.*302C>G ENSP00000261267.2:n.*302C>G
NM_000239.2:c.*302C>G , LRG_768t1:c.*302C>G NP_000230.1:n.*302C>G
NM_000239.3:c.*302C>G MANE Select NP_000230.1:n.*302C>G
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