Canonical Allele Identifier: CA385725951
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69743975T>G (hg19) chr12:g.69350195T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69350195T>G , CM000674.2:g.69350195T>G GRCh38
NC_000012.11:g.69743975T>G , CM000674.1:g.69743975T>G GRCh37
NC_000012.10:g.68030242T>G NCBI36
NG_008195.1:g.6842T>G , LRG_768:g.6842T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.224T>G MANE Select ENSP00000261267.2:p.Phe75Cys
ENST00000261267.6:c.224T>G ENSP00000261267.2:p.Phe75Cys
ENST00000548839.1:c.224T>G ENSP00000449969.1:p.Phe75Cys
ENST00000549690.1:c.224T>G ENSP00000449898.1:p.Phe75Cys
NM_000239.2:c.224T>G , LRG_768t1:c.224T>G NP_000230.1:p.Phe75Cys
NM_000239.3:c.224T>G MANE Select NP_000230.1:p.Phe75Cys
Search 100 bp 5'
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