Canonical Allele Identifier: CA406708739
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs751390677
gnomAD v2: 19-49090543-G-C
gnomAD v4: 19-48587286-G-C
MyVariant Identifiers: chr19:g.49090543G>C (hg19) chr19:g.48587286G>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.272G>C MANE Select ENSP00000201586.2:p.Trp91Ser
ENST00000201586.6:c.272G>C ENSP00000201586.1:p.Trp91Ser
ENST00000323090.4:c.227G>C ENSP00000312880.3:p.Trp76Ser
NM_004605.2:c.227G>C NP_004596.2:p.Trp76Ser
NM_177973.1:c.272G>C NP_814444.1:p.Trp91Ser
NM_177973.2:c.272G>C MANE Select NP_814444.1:p.Trp91Ser
Search 100 bp 5'
Search 100 bp 3'