Canonical Allele Identifier: CA480442693
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69743961T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69350181T>C , CM000674.2:g.69350181T>C GRCh38
NC_000012.11:g.69743961T>C , CM000674.1:g.69743961T>C GRCh37
NC_000012.10:g.68030228T>C NCBI36
NG_008195.1:g.6828T>C , LRG_768:g.6828T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.210T>C MANE Select ENSP00000261267.2:p.Thr70=
ENST00000261267.6:c.210T>C ENSP00000261267.2:p.Thr70=
ENST00000548839.1:c.210T>C ENSP00000449969.1:p.Thr70=
ENST00000549690.1:c.210T>C ENSP00000449898.1:p.Thr70=
NM_000239.2:c.210T>C , LRG_768t1:c.210T>C NP_000230.1:p.Thr70=
NM_000239.3:c.210T>C MANE Select NP_000230.1:p.Thr70=
Search 100 bp 5'
Search 100 bp 3'