Canonical Allele Identifier: CA381111569
Gene: PYGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.64526165G>C (hg19) chr11:g.64758693G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758693G>C , CM000673.2:g.64758693G>C GRCh38
NC_000011.9:g.64526165G>C , CM000673.1:g.64526165G>C GRCh37
NC_000011.8:g.64282741G>C NCBI36
NG_013018.1:g.7023C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.255C>G MANE Select ENSP00000164139.3:p.Tyr85Ter
ENST00000164139.3:c.255C>G ENSP00000164139.3:p.Tyr85Ter
ENST00000377432.7:c.244-427C>G ENSP00000366650.3:n.244-427C>G
NM_001164716.1:c.244-427C>G NP_001158188.1:n.244-427C>G
NM_005609.2:c.255C>G NP_005600.1:p.Tyr85Ter
NM_005609.3:c.255C>G NP_005600.1:p.Tyr85Ter
NM_005609.4:c.255C>G MANE Select NP_005600.1:p.Tyr85Ter
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