Canonical Allele Identifier: CA2206128148
Gene: PMM2 HGNC NCBI

Linked Data

dbSNP Id: rs1596481675
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797715T>G , CM000678.2:g.8797715T>G GRCh38
NC_000016.9:g.8891572T>G , CM000678.1:g.8891572T>G GRCh37
NC_000016.8:g.8799073T>G NCBI36
NG_009209.1:g.4903T>G
NG_033146.1:g.4934A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000566983.5:c.-15-4084T>G ENSP00000457956.1:n.-15-4084T>G
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