Canonical Allele Identifier: CA406709170
Gene: SULT2B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49090645A>C (hg19) chr19:g.48587388A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587388A>C , CM000681.2:g.48587388A>C GRCh38
NC_000019.9:g.49090645A>C , CM000681.1:g.49090645A>C GRCh37
NC_000019.8:g.53782457A>C NCBI36
NG_029063.1:g.40217A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000201586.7:c.374A>C MANE Select ENSP00000201586.2:p.His125Pro
ENST00000201586.6:c.374A>C ENSP00000201586.1:p.His125Pro
ENST00000323090.4:c.329A>C ENSP00000312880.3:p.His110Pro
NM_004605.2:c.329A>C NP_004596.2:p.His110Pro
NM_177973.1:c.374A>C NP_814444.1:p.His125Pro
NM_177973.2:c.374A>C MANE Select NP_814444.1:p.His125Pro
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