Canonical Allele Identifier: CA475161364
Gene: PYGM HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.64527224T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759752T>C , CM000673.2:g.64759752T>C GRCh38
NC_000011.9:g.64527224T>C , CM000673.1:g.64527224T>C GRCh37
NC_000011.8:g.64283800T>C NCBI36
NG_013018.1:g.5964A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.147A>G MANE Select ENSP00000164139.3:p.Pro49=
ENST00000164139.3:c.147A>G ENSP00000164139.3:p.Pro49=
ENST00000377432.7:c.147A>G ENSP00000366650.3:p.Pro49=
NM_001164716.1:c.147A>G NP_001158188.1:p.Pro49=
NM_005609.2:c.147A>G NP_005600.1:p.Pro49=
NM_005609.3:c.147A>G NP_005600.1:p.Pro49=
NM_005609.4:c.147A>G MANE Select NP_005600.1:p.Pro49=