Canonical Allele Identifier: CA7183888
Gene: PYGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2271815
ClinVar RCV Id: RCV002799504
dbSNP Id: rs771094581
ExAC: 14:51410898 T / C
gnomAD v2: 14-51410898-T-C
gnomAD v3: 14-50944180-T-C
gnomAD v4: 14-50944180-T-C
MyVariant Identifiers: chr14:g.51410898T>C (hg19) chr14:g.50944180T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50944180T>C , CM000676.2:g.50944180T>C GRCh38
NC_000014.8:g.51410898T>C , CM000676.1:g.51410898T>C GRCh37
NC_000014.7:g.50480648T>C NCBI36
NG_012796.1:g.5351A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.224A>G MANE Select ENSP00000216392.7:p.Tyr75Cys
ENST00000216392.7:c.224A>G ENSP00000216392.7:p.Tyr75Cys
ENST00000530336.2:n.291A>G
ENST00000532462.5:c.224A>G ENSP00000431657.1:p.Tyr75Cys
ENST00000544180.6:c.224A>G ENSP00000443787.1:p.Tyr75Cys
NM_001163940.1:c.224A>G NP_001157412.1:p.Tyr75Cys
NM_002863.4:c.224A>G NP_002854.3:p.Tyr75Cys
NM_002863.5:c.224A>G MANE Select NP_002854.3:p.Tyr75Cys
NM_001163940.2:c.224A>G NP_001157412.1:p.Tyr75Cys
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