Canonical Allele Identifier: CA1978928260
Gene: PYGM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758351T= , CM000673.2:g.64758351T= GRCh38
NC_000011.9:g.64525823T= , CM000673.1:g.64525823T= GRCh37
NC_000011.8:g.64282399T= NCBI36
NG_013018.1:g.7365A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.425-2A= MANE Select ENSP00000164139.3:n.425-2A=
ENST00000164139.3:c.425-2A= ENSP00000164139.3:n.425-2A=
ENST00000377432.7:c.244-85A= ENSP00000366650.3:n.244-85A=
NM_001164716.1:c.244-85A= NP_001158188.1:n.244-85A=
NM_005609.2:c.425-2A= NP_005600.1:n.425-2A=
NM_005609.3:c.425-2A= NP_005600.1:n.425-2A=
NM_005609.4:c.425-2A= MANE Select NP_005600.1:n.425-2A=
Search 100 bp 5'
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