Canonical Allele Identifier: CA432242021
Gene: GAL3ST2 HGNC NCBI

Linked Data

gnomAD v4: 2-241801859-G-C
MyVariant Identifiers: chr2:g.242741274G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241801859G>C , CM000664.2:g.241801859G>C GRCh38
NC_000002.11:g.242741274G>C , CM000664.1:g.242741274G>C GRCh37
NC_000002.10:g.242389947G>C NCBI36
NG_046977.1:g.30035G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000192314.7:c.198G>C MANE Select ENSP00000192314.6:p.Thr66=
ENST00000192314.6:c.198G>C ENSP00000192314.6:p.Thr66=
NM_022134.2:c.198G>C NP_071417.2:p.Thr66=
NM_022134.3:c.198G>C MANE Select NP_071417.2:p.Thr66=
Search 100 bp 5'
Search 100 bp 3'