Canonical Allele Identifier: CA14244983
Gene: SULT1A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1968752

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28620264T>G , CM000678.2:g.28620264T>G GRCh38
NC_000016.9:g.28631585T>G , CM000678.1:g.28631585T>G GRCh37
NC_000016.8:g.28539086T>G NCBI36
NG_028128.1:g.8282A>C

Transcript Alleles

HGVS Amino-acid change
NM_177536.3:c.68-131A>C VV NP_803880.1:p.=
XM_017023607.2:c.-136-131A>C XP_016879096.1:p.=
XM_017023611.2:c.-336-131A>C XP_016879100.1:p.=
XM_017023612.2:c.-260-131A>C XP_016879101.1:p.=
XM_017023613.2:c.-75-131A>C XP_016879102.1:p.=
XM_024450408.1:c.-136-131A>C XP_024306176.1:p.=
XM_024450409.1:c.-1239-131A>C XP_024306177.1:p.=
XM_024450410.1:c.-839-131A>C XP_024306178.1:p.=
XM_024450411.1:c.-1132-131A>C XP_024306179.1:p.=
ENST00000350842.8:c.68-131A>C ENSP00000329399.4:p.=
ENST00000395609.5:c.-336-131A>C ENSP00000378972.1:p.=
ENST00000562058.5:c.68-131A>C ENSP00000456215.1:p.=
ENST00000563493.1:c.68-131A>C ENSP00000457083.1:p.=
ENST00000564818.5:c.68-131A>C ENSP00000454388.1:p.=