Canonical Allele Identifier: CA381113184
Gene: PYGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.64527326A>C (hg19) chr11:g.64759854A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759854A>C , CM000673.2:g.64759854A>C GRCh38
NC_000011.9:g.64527326A>C , CM000673.1:g.64527326A>C GRCh37
NC_000011.8:g.64283902A>C NCBI36
NG_013018.1:g.5862T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.45T>G MANE Select ENSP00000164139.3:p.Ser15Arg
ENST00000164139.3:c.45T>G ENSP00000164139.3:p.Ser15Arg
ENST00000377432.7:c.45T>G ENSP00000366650.3:p.Ser15Arg
NM_001164716.1:c.45T>G NP_001158188.1:p.Ser15Arg
NM_005609.2:c.45T>G NP_005600.1:p.Ser15Arg
NM_005609.3:c.45T>G NP_005600.1:p.Ser15Arg
NM_005609.4:c.45T>G MANE Select NP_005600.1:p.Ser15Arg
Search 100 bp 5'
Search 100 bp 3'