Canonical Allele Identifier: CA238507307
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1033887137
MyVariant Identifiers: chr12:g.69747427C>A (hg19) chr12:g.69353647C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353647C>A , CM000674.2:g.69353647C>A GRCh38
NC_000012.11:g.69747427C>A , CM000674.1:g.69747427C>A GRCh37
NC_000012.10:g.68033694C>A NCBI36
NG_008195.1:g.10294C>A , LRG_768:g.10294C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*428C>A MANE Select ENSP00000261267.2:n.*428C>A
ENST00000261267.6:c.*428C>A ENSP00000261267.2:n.*428C>A
NM_000239.2:c.*428C>A , LRG_768t1:c.*428C>A NP_000230.1:n.*428C>A
NM_000239.3:c.*428C>A MANE Select NP_000230.1:n.*428C>A
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