Canonical Allele Identifier: CA948901598
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1874896126

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353622G>T , CM000674.2:g.69353622G>T GRCh38
NC_000012.11:g.69747402G>T , CM000674.1:g.69747402G>T GRCh37
NC_000012.10:g.68033669G>T NCBI36
NG_008195.1:g.10269G>T , LRG_768:g.10269G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*403G>T MANE Select ENSP00000261267.2:n.*403G>T
ENST00000261267.6:c.*403G>T ENSP00000261267.2:n.*403G>T
NM_000239.2:c.*403G>T , LRG_768t1:c.*403G>T NP_000230.1:n.*403G>T
NM_000239.3:c.*403G>T MANE Select NP_000230.1:n.*403G>T