Canonical Allele Identifier: CA238507317
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1043400200
gnomAD v4: 12-69353655-A-T
MyVariant Identifiers: chr12:g.69747435A>T (hg19) chr12:g.69353655A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353655A>T , CM000674.2:g.69353655A>T GRCh38
NC_000012.11:g.69747435A>T , CM000674.1:g.69747435A>T GRCh37
NC_000012.10:g.68033702A>T NCBI36
NG_008195.1:g.10302A>T , LRG_768:g.10302A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*436A>T MANE Select ENSP00000261267.2:n.*436A>T
ENST00000261267.6:c.*436A>T ENSP00000261267.2:n.*436A>T
NM_000239.2:c.*436A>T , LRG_768t1:c.*436A>T NP_000230.1:n.*436A>T
NM_000239.3:c.*436A>T MANE Select NP_000230.1:n.*436A>T
Search 100 bp 5'
Search 100 bp 3'