Canonical Allele Identifier: CA279794099

Gene: SULT1A1

Linked Data

• dbSNP Id: rs899502202
• gnomAD v3: 16-28620184-A-G
• gnomAD v4: 16-28620184-A-G
• MyVariant Identifiers: chr16:g.28631505A>G (hg19) ; chr16:g.28620184A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.28620184A>G , CM000678.2:g.28620184A>G	GRCh38
NC_000016.9:g.28631505A>G , CM000678.1:g.28631505A>G	GRCh37
NC_000016.8:g.28539006A>G	NCBI36
NG_028128.1:g.8362T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698935.1:n.353-51T>C
ENST00000395607.6:c.68-51T>C	ENSP00000378971.2:n.68-51T>C
ENST00000395609.6:n.426-51T>C
ENST00000677940.1:c.68-51T>C	ENSP00000503077.1:n.68-51T>C
ENST00000679262.1:c.*48-51T>C	ENSP00000502863.1:n.*48-51T>C
ENST00000350842.8:c.68-51T>C	ENSP00000329399.4:n.68-51T>C
ENST00000395609.5:c.-336-51T>C	ENSP00000378972.1:n.-336-51T>C
ENST00000562058.5:c.68-51T>C	ENSP00000456215.1:n.68-51T>C
ENST00000563493.1:c.68-51T>C	ENSP00000457083.1:n.68-51T>C
ENST00000564818.5:c.68-51T>C	ENSP00000454388.1:n.68-51T>C
NM_177536.3:c.68-51T>C	NP_803880.1:n.68-51T>C
XM_017023607.2:c.-136-51T>C	XP_016879096.1:n.-136-51T>C
XM_017023611.2:c.-336-51T>C	XP_016879100.1:n.-336-51T>C
XM_017023612.2:c.-260-51T>C	XP_016879101.1:n.-260-51T>C
XM_017023613.2:c.-75-51T>C	XP_016879102.1:n.-75-51T>C
XM_024450408.1:c.-136-51T>C	XP_024306176.1:n.-136-51T>C
XM_024450409.1:c.-1239-51T>C	XP_024306177.1:n.-1239-51T>C
XM_024450410.1:c.-839-51T>C	XP_024306178.1:n.-839-51T>C
XM_024450411.1:c.-1132-51T>C	XP_024306179.1:n.-1132-51T>C
NM_177536.4:c.68-51T>C	NP_803880.1:n.68-51T>C
NM_001394421.1:c.-409-51T>C	NP_001381350.1:n.-409-51T>C
NM_001394422.1:c.-1208-51T>C	NP_001381351.1:n.-1208-51T>C
NM_001394423.1:c.-539-51T>C	NP_001381352.1:n.-539-51T>C
NM_001394424.1:c.-106-51T>C	NP_001381353.1:n.-106-51T>C
NM_001394425.1:c.-336-51T>C	NP_001381354.1:n.-336-51T>C
NM_177536.5:c.-2-51T>C	NP_803880.2:n.-2-51T>C