Canonical Allele Identifier: CA2136419323
Gene: PYGL HGNC NCBI

Linked Data

dbSNP Id: rs2050441771
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50915796A>G , CM000676.2:g.50915796A>G GRCh38
NC_000014.8:g.51382514A>G , CM000676.1:g.51382514A>G GRCh37
NC_000014.7:g.50452264A>G NCBI36
NG_012796.1:g.33735T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216392.8:c.1239+29T>C MANE Select ENSP00000216392.7:n.1239+29T>C
ENST00000216392.7:c.1239+29T>C ENSP00000216392.7:n.1239+29T>C
ENST00000528757.2:n.116+29T>C
ENST00000532462.5:c.1239+29T>C ENSP00000431657.1:n.1239+29T>C
ENST00000544180.6:c.1137+29T>C ENSP00000443787.1:n.1137+29T>C
NM_001163940.1:c.1137+29T>C NP_001157412.1:n.1137+29T>C
NM_002863.4:c.1239+29T>C NP_002854.3:n.1239+29T>C
NM_002863.5:c.1239+29T>C MANE Select NP_002854.3:n.1239+29T>C
NM_001163940.2:c.1137+29T>C NP_001157412.1:n.1137+29T>C
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