Canonical Allele Identifier: CA2631641632
Gene: PMM2 HGNC NCBI

Linked Data

gnomAD v4: 16-8797747-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797747C>T , CM000678.2:g.8797747C>T GRCh38
NC_000016.9:g.8891604C>T , CM000678.1:g.8891604C>T GRCh37
NC_000016.8:g.8799105C>T NCBI36
NG_009209.1:g.4935C>T
NG_033146.1:g.4902G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682008.1:c.-136C>T ENSP00000507849.1:n.-136C>T
ENST00000566983.5:c.-15-4052C>T ENSP00000457956.1:n.-15-4052C>T
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