Canonical Allele Identifier: CA351416611
Gene: GAL3ST2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.242741228T>C (hg19) chr2:g.241801813T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241801813T>C , CM000664.2:g.241801813T>C GRCh38
NC_000002.11:g.242741228T>C , CM000664.1:g.242741228T>C GRCh37
NC_000002.10:g.242389901T>C NCBI36
NG_046977.1:g.29989T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000192314.7:c.152T>C MANE Select ENSP00000192314.6:p.Val51Ala
ENST00000192314.6:c.152T>C ENSP00000192314.6:p.Val51Ala
NM_022134.2:c.152T>C NP_071417.2:p.Val51Ala
NM_022134.3:c.152T>C MANE Select NP_071417.2:p.Val51Ala
Search 100 bp 5'
Search 100 bp 3'