Canonical Allele Identifier: CA223899625

Gene: PYGM

Linked Data

• dbSNP Id: rs920965348
• gnomAD v3: 11-64752722-C-A
• gnomAD v4: 11-64752722-C-A
• MyVariant Identifiers: chr11:g.64752722C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64752722C>A , CM000673.2:g.64752722C>A	GRCh38
NC_000011.9:g.64520194C>A , CM000673.1:g.64520194C>A	GRCh37
NC_000011.8:g.64276770C>A	NCBI36
NG_013018.1:g.12994G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000164139.4:c.1519-218G>T MANE Select	ENSP00000164139.3:n.1519-218G>T
ENST00000164139.3:c.1519-218G>T	ENSP00000164139.3:n.1519-218G>T
ENST00000377432.7:c.1255-218G>T	ENSP00000366650.3:n.1255-218G>T
NM_001164716.1:c.1255-218G>T	NP_001158188.1:n.1255-218G>T
NM_005609.2:c.1519-218G>T	NP_005600.1:n.1519-218G>T
NM_005609.3:c.1519-218G>T	NP_005600.1:n.1519-218G>T
NM_005609.4:c.1519-218G>T MANE Select	NP_005600.1:n.1519-218G>T