Canonical Allele Identifier: CA9553036
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs751390677
ExAC: 19:49090543 G / T
gnomAD v2: 19-49090543-G-T
gnomAD v4: 19-48587286-G-T
MyVariant Identifiers: chr19:g.49090543G>T (hg19) chr19:g.48587286G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587286G>T , CM000681.2:g.48587286G>T GRCh38
NC_000019.9:g.49090543G>T , CM000681.1:g.49090543G>T GRCh37
NC_000019.8:g.53782355G>T NCBI36
NG_029063.1:g.40115G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.272G>T MANE Select ENSP00000201586.2:p.Trp91Leu
ENST00000201586.6:c.272G>T ENSP00000201586.1:p.Trp91Leu
ENST00000323090.4:c.227G>T ENSP00000312880.3:p.Trp76Leu
NM_004605.2:c.227G>T NP_004596.2:p.Trp76Leu
NM_177973.1:c.272G>T NP_814444.1:p.Trp91Leu
NM_177973.2:c.272G>T MANE Select NP_814444.1:p.Trp91Leu
Search 100 bp 5'
Search 100 bp 3'