Canonical Allele Identifier: CA480443069
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69747360C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353580C>G , CM000674.2:g.69353580C>G GRCh38
NC_000012.11:g.69747360C>G , CM000674.1:g.69747360C>G GRCh37
NC_000012.10:g.68033627C>G NCBI36
NG_008195.1:g.10227C>G , LRG_768:g.10227C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*361C>G MANE Select ENSP00000261267.2:n.*361C>G
ENST00000261267.6:c.*361C>G ENSP00000261267.2:n.*361C>G
NM_000239.2:c.*361C>G , LRG_768t1:c.*361C>G NP_000230.1:n.*361C>G
NM_000239.3:c.*361C>G MANE Select NP_000230.1:n.*361C>G