Canonical Allele Identifier: CA474960022

Gene: PYGM

Linked Data

• MyVariant Identifiers: chr11:g.64525769C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64758297C>G , CM000673.2:g.64758297C>G	GRCh38
NC_000011.9:g.64525769C>G , CM000673.1:g.64525769C>G	GRCh37
NC_000011.8:g.64282345C>G	NCBI36
NG_013018.1:g.7419G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.477G>C MANE Select	ENSP00000164139.3:p.Gly159=
ENST00000164139.3:c.477G>C	ENSP00000164139.3:p.Gly159=
ENST00000377432.7:c.244-31G>C	ENSP00000366650.3:n.244-31G>C
NM_001164716.1:c.244-31G>C	NP_001158188.1:n.244-31G>C
NM_005609.2:c.477G>C	NP_005600.1:p.Gly159=
NM_005609.3:c.477G>C	NP_005600.1:p.Gly159=
NM_005609.4:c.477G>C MANE Select	NP_005600.1:p.Gly159=