Canonical Allele Identifier: CA238507334
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs919441242
gnomAD v2: 12-69747449-T-C
gnomAD v3: 12-69353669-T-C
gnomAD v4: 12-69353669-T-C
MyVariant Identifiers: chr12:g.69747449T>C (hg19) chr12:g.69353669T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353669T>C , CM000674.2:g.69353669T>C GRCh38
NC_000012.11:g.69747449T>C , CM000674.1:g.69747449T>C GRCh37
NC_000012.10:g.68033716T>C NCBI36
NG_008195.1:g.10316T>C , LRG_768:g.10316T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*450T>C MANE Select ENSP00000261267.2:n.*450T>C
ENST00000261267.6:c.*450T>C ENSP00000261267.2:n.*450T>C
NM_000239.2:c.*450T>C , LRG_768t1:c.*450T>C NP_000230.1:n.*450T>C
NM_000239.3:c.*450T>C MANE Select NP_000230.1:n.*450T>C
Search 100 bp 5'
Search 100 bp 3'