Canonical Allele Identifier: CA534692611

Gene: SULT1C4

Linked Data

• dbSNP Id: rs1246340740
• gnomAD v2: 2-109003669-G-A
• gnomAD v3: 2-108387213-G-A
• gnomAD v4: 2-108387213-G-A
• MyVariant Identifiers: chr2:g.109003669G>A (hg19) ; chr2:g.108387213G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108387213G>A , CM000664.2:g.108387213G>A	GRCh38
NC_000002.11:g.109003669G>A , CM000664.1:g.109003669G>A	GRCh37
NC_000002.10:g.108370101G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.797-107G>A MANE Select	ENSP00000272452.2:n.797-107G>A
ENST00000272452.6:c.797-107G>A	ENSP00000272452.2:n.797-107G>A
ENST00000409309.3:c.572-107G>A	ENSP00000387225.3:n.572-107G>A
NM_006588.2:c.797-107G>A	NP_006579.2:n.797-107G>A
XM_005263919.2:c.572-107G>A	XP_005263976.1:n.572-107G>A
NM_001321770.1:c.572-107G>A	NP_001308699.1:n.572-107G>A
NM_006588.3:c.797-107G>A	NP_006579.2:n.797-107G>A
NR_135776.1:n.1049-107G>A
NR_135779.1:n.778-107G>A
XM_017003807.1:c.527-107G>A	XP_016859296.1:n.527-107G>A
NM_006588.4:c.797-107G>A MANE Select	NP_006579.2:n.797-107G>A
NM_001321770.2:c.572-107G>A	NP_001308699.1:n.572-107G>A
NR_135776.2:n.1006-107G>A
NR_135779.2:n.735-107G>A