Canonical Allele Identifier: CA406708891
Gene: SULT2B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49090580G>A (hg19) chr19:g.48587323G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587323G>A , CM000681.2:g.48587323G>A GRCh38
NC_000019.9:g.49090580G>A , CM000681.1:g.49090580G>A GRCh37
NC_000019.8:g.53782392G>A NCBI36
NG_029063.1:g.40152G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.309G>A MANE Select ENSP00000201586.2:p.Trp103Ter
ENST00000201586.6:c.309G>A ENSP00000201586.1:p.Trp103Ter
ENST00000323090.4:c.264G>A ENSP00000312880.3:p.Trp88Ter
NM_004605.2:c.264G>A NP_004596.2:p.Trp88Ter
NM_177973.1:c.309G>A NP_814444.1:p.Trp103Ter
NM_177973.2:c.309G>A MANE Select NP_814444.1:p.Trp103Ter
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Search 100 bp 3'