Canonical Allele Identifier: CA1978928058
Gene: PYGM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758237G= , CM000673.2:g.64758237G= GRCh38
NC_000011.9:g.64525709G= , CM000673.1:g.64525709G= GRCh37
NC_000011.8:g.64282285G= NCBI36
NG_013018.1:g.7479C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.528+9C= MANE Select ENSP00000164139.3:n.528+9C=
ENST00000164139.3:c.528+9C= ENSP00000164139.3:n.528+9C=
ENST00000377432.7:c.264+9C= ENSP00000366650.3:n.264+9C=
NM_001164716.1:c.264+9C= NP_001158188.1:n.264+9C=
NM_005609.2:c.528+9C= NP_005600.1:n.528+9C=
NM_005609.3:c.528+9C= NP_005600.1:n.528+9C=
NM_005609.4:c.528+9C= MANE Select NP_005600.1:n.528+9C=
Search 100 bp 5'
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