Canonical Allele Identifier: CA351416677
Gene: GAL3ST2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.242741260A>C (hg19) chr2:g.241801845A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241801845A>C , CM000664.2:g.241801845A>C GRCh38
NC_000002.11:g.242741260A>C , CM000664.1:g.242741260A>C GRCh37
NC_000002.10:g.242389933A>C NCBI36
NG_046977.1:g.30021A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000192314.7:c.184A>C MANE Select ENSP00000192314.6:p.Thr62Pro
ENST00000192314.6:c.184A>C ENSP00000192314.6:p.Thr62Pro
NM_022134.2:c.184A>C NP_071417.2:p.Thr62Pro
NM_022134.3:c.184A>C MANE Select NP_071417.2:p.Thr62Pro
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Search 100 bp 3'