Canonical Allele Identifier: CA385725639
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69743908G>C (hg19) chr12:g.69350128G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69350128G>C , CM000674.2:g.69350128G>C GRCh38
NC_000012.11:g.69743908G>C , CM000674.1:g.69743908G>C GRCh37
NC_000012.10:g.68030175G>C NCBI36
NG_008195.1:g.6775G>C , LRG_768:g.6775G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261267.7:c.157G>C MANE Select ENSP00000261267.2:p.Glu53Gln
ENST00000261267.6:c.157G>C ENSP00000261267.2:p.Glu53Gln
ENST00000548839.1:c.157G>C ENSP00000449969.1:p.Glu53Gln
ENST00000549690.1:c.157G>C ENSP00000449898.1:p.Glu53Gln
NM_000239.2:c.157G>C , LRG_768t1:c.157G>C NP_000230.1:p.Glu53Gln
NM_000239.3:c.157G>C MANE Select NP_000230.1:p.Glu53Gln
Search 100 bp 5'
Search 100 bp 3'