Canonical Allele Identifier: CA2624828921
Gene: PYGL HGNC NCBI

Linked Data

gnomAD v4: 14-50937902-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50937902C>T , CM000676.2:g.50937902C>T GRCh38
NC_000014.8:g.51404620C>T , CM000676.1:g.51404620C>T GRCh37
NC_000014.7:g.50474370C>T NCBI36
NG_012796.1:g.11629G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.244-65G>A MANE Select ENSP00000216392.7:n.244-65G>A
ENST00000216392.7:c.244-65G>A ENSP00000216392.7:n.244-65G>A
ENST00000530336.2:n.311-65G>A
ENST00000532462.5:c.244-65G>A ENSP00000431657.1:n.244-65G>A
ENST00000544180.6:c.244-2717G>A ENSP00000443787.1:n.244-2717G>A
NM_001163940.1:c.244-2717G>A NP_001157412.1:n.244-2717G>A
NM_002863.4:c.244-65G>A NP_002854.3:n.244-65G>A
NM_002863.5:c.244-65G>A MANE Select NP_002854.3:n.244-65G>A
NM_001163940.2:c.244-2717G>A NP_001157412.1:n.244-2717G>A
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