Canonical Allele Identifier: CA2614193516
Gene: PYGM HGNC NCBI

Linked Data

gnomAD v4: 11-64751848-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64751848T>A , CM000673.2:g.64751848T>A GRCh38
NC_000011.9:g.64519320T>A , CM000673.1:g.64519320T>A GRCh37
NC_000011.8:g.64275896T>A NCBI36
NG_013018.1:g.13868A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.1768+76A>T MANE Select ENSP00000164139.3:n.1768+76A>T
ENST00000164139.3:c.1768+76A>T ENSP00000164139.3:n.1768+76A>T
ENST00000377432.7:c.1504+76A>T ENSP00000366650.3:n.1504+76A>T
ENST00000462303.1:n.92+76A>T
NM_001164716.1:c.1504+76A>T NP_001158188.1:n.1504+76A>T
NM_005609.2:c.1768+76A>T NP_005600.1:n.1768+76A>T
NM_005609.3:c.1768+76A>T NP_005600.1:n.1768+76A>T
NM_005609.4:c.1768+76A>T MANE Select NP_005600.1:n.1768+76A>T
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