Canonical Allele Identifier: CA706633017
Gene: PYGL HGNC NCBI

Linked Data

dbSNP Id: rs1330373770
MyVariant Identifiers: chr14:g.51411206del (hg19) chr14:g.50944488del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50944488del , CM000676.2:g.50944488del GRCh38
NC_000014.8:g.51411206del , CM000676.1:g.51411206del GRCh37
NC_000014.7:g.50480956del NCBI36
NG_012796.1:g.5043del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.7:c.-85del ENSP00000216392.7:n.-85del
NM_001163940.1:c.-85del NP_001157412.1:n.-85del
NM_002863.4:c.-85del NP_002854.3:n.-85del
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