Canonical Allele Identifier: CA432241899
Gene: GAL3ST2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.242741199G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241801784G>T , CM000664.2:g.241801784G>T GRCh38
NC_000002.11:g.242741199G>T , CM000664.1:g.242741199G>T GRCh37
NC_000002.10:g.242389872G>T NCBI36
NG_046977.1:g.29960G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000192314.7:c.123G>T MANE Select ENSP00000192314.6:p.Leu41=
ENST00000192314.6:c.123G>T ENSP00000192314.6:p.Leu41=
NM_022134.2:c.123G>T NP_071417.2:p.Leu41=
NM_022134.3:c.123G>T MANE Select NP_071417.2:p.Leu41=
Search 100 bp 5'
Search 100 bp 3'