Canonical Allele Identifier: CA474958693
Gene: PYGM HGNC NCBI

Linked Data

dbSNP Id: rs1398695723
MyVariant Identifiers: chr11:g.64517988G>A (hg19) chr11:g.64750516G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64750516G>A , CM000673.2:g.64750516G>A GRCh38
NC_000011.9:g.64517988G>A , CM000673.1:g.64517988G>A GRCh37
NC_000011.8:g.64274564G>A NCBI36
NG_013018.1:g.15200C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.2037C>T MANE Select ENSP00000164139.3:p.Asn679=
ENST00000164139.3:c.2037C>T ENSP00000164139.3:p.Asn679=
ENST00000377432.7:c.1773C>T ENSP00000366650.3:p.Asn591=
NM_001164716.1:c.1773C>T NP_001158188.1:p.Asn591=
NM_005609.2:c.2037C>T NP_005600.1:p.Asn679=
NM_005609.3:c.2037C>T NP_005600.1:p.Asn679=
NM_005609.4:c.2037C>T MANE Select NP_005600.1:p.Asn679=
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