Canonical Allele Identifier: CA381111869
Gene: PYGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.64527136C>T (hg19) chr11:g.64759664C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759664C>T , CM000673.2:g.64759664C>T GRCh38
NC_000011.9:g.64527136C>T , CM000673.1:g.64527136C>T GRCh37
NC_000011.8:g.64283712C>T NCBI36
NG_013018.1:g.6052G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.235G>A MANE Select ENSP00000164139.3:p.Asp79Asn
ENST00000164139.3:c.235G>A ENSP00000164139.3:p.Asp79Asn
ENST00000377432.7:c.235G>A ENSP00000366650.3:p.Asp79Asn
NM_001164716.1:c.235G>A NP_001158188.1:p.Asp79Asn
NM_005609.2:c.235G>A NP_005600.1:p.Asp79Asn
NM_005609.3:c.235G>A NP_005600.1:p.Asp79Asn
NM_005609.4:c.235G>A MANE Select NP_005600.1:p.Asp79Asn
Search 100 bp 5'
Search 100 bp 3'