Canonical Allele Identifier: CA480442710
Gene: LYZ HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.69744003T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69350223T>C , CM000674.2:g.69350223T>C GRCh38
NC_000012.11:g.69744003T>C , CM000674.1:g.69744003T>C GRCh37
NC_000012.10:g.68030270T>C NCBI36
NG_008195.1:g.6870T>C , LRG_768:g.6870T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.252T>C MANE Select ENSP00000261267.2:p.Asn84=
ENST00000261267.6:c.252T>C ENSP00000261267.2:p.Asn84=
ENST00000548839.1:c.252T>C ENSP00000449969.1:p.Asn84=
ENST00000549690.1:c.252T>C ENSP00000449898.1:p.Asn84=
NM_000239.2:c.252T>C , LRG_768t1:c.252T>C NP_000230.1:p.Asn84=
NM_000239.3:c.252T>C MANE Select NP_000230.1:p.Asn84=