Canonical Allele Identifier: CA406708730

Gene: SULT2B1

Linked Data

• gnomAD v4: 19-48587283-C-T
• MyVariant Identifiers: chr19:g.49090540C>T (hg19) ; chr19:g.48587283C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48587283C>T , CM000681.2:g.48587283C>T	GRCh38
NC_000019.9:g.49090540C>T , CM000681.1:g.49090540C>T	GRCh37
NC_000019.8:g.53782352C>T	NCBI36
NG_029063.1:g.40112C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000201586.7:c.269C>T MANE Select	ENSP00000201586.2:p.Ser90Phe
ENST00000201586.6:c.269C>T	ENSP00000201586.1:p.Ser90Phe
ENST00000323090.4:c.224C>T	ENSP00000312880.3:p.Ser75Phe
NM_004605.2:c.224C>T	NP_004596.2:p.Ser75Phe
NM_177973.1:c.269C>T	NP_814444.1:p.Ser90Phe
NM_177973.2:c.269C>T MANE Select	NP_814444.1:p.Ser90Phe