Canonical Allele Identifier: CA1304728080
Gene: GALNT3 HGNC NCBI

Linked Data

dbSNP Id: rs1688287050
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165747866A>T , CM000664.2:g.165747866A>T GRCh38
NC_000002.11:g.166604376A>T , CM000664.1:g.166604376A>T GRCh37
NC_000002.10:g.166312622A>T NCBI36
NG_012069.1:g.51428T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392701.8:c.*915T>A MANE Select ENSP00000376465.3:n.*915T>A
ENST00000392701.7:c.*915T>A ENSP00000376465.3:n.*915T>A
ENST00000409882.5:c.*915T>A ENSP00000386955.1:n.*915T>A
NM_004482.3:c.*915T>A NP_004473.2:n.*915T>A
XM_005246449.1:c.*915T>A XP_005246506.1:n.*915T>A
XM_011510929.1:c.*915T>A XP_011509231.1:n.*915T>A
XM_017003770.1:c.*915T>A XP_016859259.1:n.*915T>A
NM_004482.4:c.*915T>A MANE Select NP_004473.2:n.*915T>A
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