Canonical Allele Identifier: CA2727001921
Gene: GNPTAB HGNC NCBI

Linked Data

dbSNP Id: rs2137198557
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.101830936T>G , CM000674.2:g.101830936T>G GRCh38
NC_000012.11:g.102224714T>G , CM000674.1:g.102224714T>G GRCh37
NC_000012.10:g.100748845T>G NCBI36
NG_021243.1:g.4932A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299314.12:c.-261A>C MANE Select ENSP00000299314.7:n.-261A>C
ENST00000299314.11:c.-261A>C ENSP00000299314.7:n.-261A>C
NM_024312.5:c.-261A>C MANE Select NP_077288.2:n.-261A>C
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