Canonical Allele Identifier: CA2724511996
Gene: PYGM HGNC NCBI

Linked Data

dbSNP Id: rs2135843044
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759934A>G , CM000673.2:g.64759934A>G GRCh38
NC_000011.9:g.64527406A>G , CM000673.1:g.64527406A>G GRCh37
NC_000011.8:g.64283982A>G NCBI36
NG_013018.1:g.5782T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-36T>C MANE Select ENSP00000164139.3:n.-36T>C
ENST00000164139.3:c.-36T>C ENSP00000164139.3:n.-36T>C
ENST00000377432.7:c.-36T>C ENSP00000366650.3:n.-36T>C
NM_001164716.1:c.-36T>C NP_001158188.1:n.-36T>C
NM_005609.2:c.-36T>C NP_005600.1:n.-36T>C
NM_005609.3:c.-36T>C NP_005600.1:n.-36T>C
NM_005609.4:c.-36T>C MANE Select NP_005600.1:n.-36T>C
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