Canonical Allele Identifier: CA381167615
Gene: PYGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.64517899A>G (hg19) chr11:g.64750427A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64750427A>G , CM000673.2:g.64750427A>G GRCh38
NC_000011.9:g.64517899A>G , CM000673.1:g.64517899A>G GRCh37
NC_000011.8:g.64274475A>G NCBI36
NG_007574.1:g.30T>C , LRG_100:g.30T>C
NG_013018.1:g.15289T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.2126T>C MANE Select ENSP00000164139.3:p.Phe709Ser
ENST00000164139.3:c.2126T>C ENSP00000164139.3:p.Phe709Ser
ENST00000377432.7:c.1862T>C ENSP00000366650.3:p.Phe621Ser
NM_001164716.1:c.1862T>C NP_001158188.1:p.Phe621Ser
NM_005609.2:c.2126T>C NP_005600.1:p.Phe709Ser
NM_005609.3:c.2126T>C NP_005600.1:p.Phe709Ser
NM_005609.4:c.2126T>C MANE Select NP_005600.1:p.Phe709Ser
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