Canonical Allele Identifier: CA238507239
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs997971111
gnomAD v2: 12-69747369-C-T
gnomAD v3: 12-69353589-C-T
gnomAD v4: 12-69353589-C-T
MyVariant Identifiers: chr12:g.69747369C>T (hg19) chr12:g.69353589C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353589C>T , CM000674.2:g.69353589C>T GRCh38
NC_000012.11:g.69747369C>T , CM000674.1:g.69747369C>T GRCh37
NC_000012.10:g.68033636C>T NCBI36
NG_008195.1:g.10236C>T , LRG_768:g.10236C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*370C>T MANE Select ENSP00000261267.2:n.*370C>T
ENST00000261267.6:c.*370C>T ENSP00000261267.2:n.*370C>T
NM_000239.2:c.*370C>T , LRG_768t1:c.*370C>T NP_000230.1:n.*370C>T
NM_000239.3:c.*370C>T MANE Select NP_000230.1:n.*370C>T
Search 100 bp 5'
Search 100 bp 3'