Canonical Allele Identifier: CA682766111
Gene: GNPTAB HGNC NCBI

Linked Data

dbSNP Id: rs1213609982
gnomAD v3: 12-101830890-G-T
gnomAD v4: 12-101830890-G-T
MyVariant Identifiers: chr12:g.102224668G>T (hg19) chr12:g.101830890G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101830890G>T , CM000674.2:g.101830890G>T GRCh38
NC_000012.11:g.102224668G>T , CM000674.1:g.102224668G>T GRCh37
NC_000012.10:g.100748799G>T NCBI36
NG_021243.1:g.4978C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.-215C>A MANE Select ENSP00000299314.7:n.-215C>A
ENST00000299314.11:c.-215C>A ENSP00000299314.7:n.-215C>A
NM_024312.5:c.-215C>A MANE Select NP_077288.2:n.-215C>A
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