Canonical Allele Identifier: CA406708754
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs1479363064
gnomAD v2: 19-49090546-T-C
gnomAD v3: 19-48587289-T-C
gnomAD v4: 19-48587289-T-C
MyVariant Identifiers: chr19:g.49090546T>C (hg19) chr19:g.48587289T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587289T>C , CM000681.2:g.48587289T>C GRCh38
NC_000019.9:g.49090546T>C , CM000681.1:g.49090546T>C GRCh37
NC_000019.8:g.53782358T>C NCBI36
NG_029063.1:g.40118T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.275T>C MANE Select ENSP00000201586.2:p.Ile92Thr
ENST00000201586.6:c.275T>C ENSP00000201586.1:p.Ile92Thr
ENST00000323090.4:c.230T>C ENSP00000312880.3:p.Ile77Thr
NM_004605.2:c.230T>C NP_004596.2:p.Ile77Thr
NM_177973.1:c.275T>C NP_814444.1:p.Ile92Thr
NM_177973.2:c.275T>C MANE Select NP_814444.1:p.Ile92Thr
Search 100 bp 5'
Search 100 bp 3'