Canonical Allele Identifier: CA389678922
Gene: PYGL HGNC NCBI

Linked Data

dbSNP Id: rs2142781794

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50905456T>C , CM000676.2:g.50905456T>C GRCh38
NC_000014.8:g.51372174T>C , CM000676.1:g.51372174T>C GRCh37
NC_000014.7:g.50441924T>C NCBI36
NG_012796.1:g.44075A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.2480A>G MANE Select ENSP00000216392.7:p.Asn827Ser
ENST00000216392.7:c.2480A>G ENSP00000216392.7:p.Asn827Ser
ENST00000532462.5:c.2379+2815A>G ENSP00000431657.1:n.2379+2815A>G
ENST00000544180.6:c.2378A>G ENSP00000443787.1:p.Asn793Ser
NM_001163940.1:c.2378A>G NP_001157412.1:p.Asn793Ser
NM_002863.4:c.2480A>G NP_002854.3:p.Asn827Ser
NM_002863.5:c.2480A>G MANE Select NP_002854.3:p.Asn827Ser
NM_001163940.2:c.2378A>G NP_001157412.1:p.Asn793Ser