Canonical Allele Identifier: CA480442875
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1874892887
gnomAD v4: 12-69353514-A-G
MyVariant Identifiers: chr12:g.69747294A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353514A>G , CM000674.2:g.69353514A>G GRCh38
NC_000012.11:g.69747294A>G , CM000674.1:g.69747294A>G GRCh37
NC_000012.10:g.68033561A>G NCBI36
NG_008195.1:g.10161A>G , LRG_768:g.10161A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*295A>G MANE Select ENSP00000261267.2:n.*295A>G
ENST00000261267.6:c.*295A>G ENSP00000261267.2:n.*295A>G
NM_000239.2:c.*295A>G , LRG_768t1:c.*295A>G NP_000230.1:n.*295A>G
NM_000239.3:c.*295A>G MANE Select NP_000230.1:n.*295A>G
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Search 100 bp 3'