Canonical Allele Identifier: CA406709441
Gene: SULT2B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49090694G>C (hg19) chr19:g.48587437G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587437G>C , CM000681.2:g.48587437G>C GRCh38
NC_000019.9:g.49090694G>C , CM000681.1:g.49090694G>C GRCh37
NC_000019.8:g.53782506G>C NCBI36
NG_029063.1:g.40266G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423G>C MANE Select ENSP00000201586.2:p.Lys141Asn
ENST00000201586.6:c.423G>C ENSP00000201586.1:p.Lys141Asn
ENST00000323090.4:c.378G>C ENSP00000312880.3:p.Lys126Asn
NM_004605.2:c.378G>C NP_004596.2:p.Lys126Asn
NM_177973.1:c.423G>C NP_814444.1:p.Lys141Asn
NM_177973.2:c.423G>C MANE Select NP_814444.1:p.Lys141Asn
Search 100 bp 5'
Search 100 bp 3'