Canonical Allele Identifier: CA59743496

Gene: GALNT3

Linked Data

• dbSNP Id: rs903709674
• gnomAD v3: 2-165751175-T-C
• gnomAD v4: 2-165751175-T-C
• MyVariant Identifiers: chr2:g.166607685T>C (hg19) ; chr2:g.165751175T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165751175T>C , CM000664.2:g.165751175T>C	GRCh38
NC_000002.11:g.166607685T>C , CM000664.1:g.166607685T>C	GRCh37
NC_000002.10:g.166315931T>C	NCBI36
NG_012069.1:g.48119A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000392701.8:c.1627-1281A>G MANE Select	ENSP00000376465.3:n.1627-1281A>G
ENST00000392701.7:c.1627-1281A>G	ENSP00000376465.3:n.1627-1281A>G
ENST00000409882.5:c.841-1281A>G	ENSP00000386955.1:n.841-1281A>G
NM_004482.3:c.1627-1281A>G	NP_004473.2:n.1627-1281A>G
XM_005246449.1:c.1627-1281A>G	XP_005246506.1:n.1627-1281A>G
XM_011510929.1:c.1627-1281A>G	XP_011509231.1:n.1627-1281A>G
XM_017003770.1:c.1627-1281A>G	XP_016859259.1:n.1627-1281A>G
XR_002959253.1:n.1903-1281A>G
NM_004482.4:c.1627-1281A>G MANE Select	NP_004473.2:n.1627-1281A>G