Canonical Allele Identifier: CA1978930052
Gene: PYGM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759868T= , CM000673.2:g.64759868T= GRCh38
NC_000011.9:g.64527340T= , CM000673.1:g.64527340T= GRCh37
NC_000011.8:g.64283916T= NCBI36
NG_013018.1:g.5848A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.31A= MANE Select ENSP00000164139.3:p.Arg11=
ENST00000164139.3:c.31A= ENSP00000164139.3:p.Arg11=
ENST00000377432.7:c.31A= ENSP00000366650.3:p.Arg11=
NM_001164716.1:c.31A= NP_001158188.1:p.Arg11=
NM_005609.2:c.31A= NP_005600.1:p.Arg11=
NM_005609.3:c.31A= NP_005600.1:p.Arg11=
NM_005609.4:c.31A= MANE Select NP_005600.1:p.Arg11=
Search 100 bp 5'
Search 100 bp 3'