Canonical Allele Identifier: CA223889522
Gene: PYGM HGNC NCBI

Linked Data

dbSNP Id: rs193179721
gnomAD v2: 11-64527417-C-A
gnomAD v3: 11-64759945-C-A
gnomAD v4: 11-64759945-C-A
MyVariant Identifiers: chr11:g.64527417C>A (hg19) chr11:g.64759945C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759945C>A , CM000673.2:g.64759945C>A GRCh38
NC_000011.9:g.64527417C>A , CM000673.1:g.64527417C>A GRCh37
NC_000011.8:g.64283993C>A NCBI36
NG_013018.1:g.5771G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.-47G>T MANE Select ENSP00000164139.3:n.-47G>T
ENST00000164139.3:c.-47G>T ENSP00000164139.3:n.-47G>T
ENST00000377432.7:c.-47G>T ENSP00000366650.3:n.-47G>T
NM_001164716.1:c.-47G>T NP_001158188.1:n.-47G>T
NM_005609.2:c.-47G>T NP_005600.1:n.-47G>T
NM_005609.3:c.-47G>T NP_005600.1:n.-47G>T
NM_005609.4:c.-47G>T MANE Select NP_005600.1:n.-47G>T
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