Canonical Allele Identifier: CA2586212637
Gene: SULT2B1 HGNC NCBI

Linked Data

gnomAD v4: 19-48587586-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587586T>G , CM000681.2:g.48587586T>G GRCh38
NC_000019.9:g.49090843T>G , CM000681.1:g.49090843T>G GRCh37
NC_000019.8:g.53782655T>G NCBI36
NG_029063.1:g.40415T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+149T>G MANE Select ENSP00000201586.2:n.423+149T>G
ENST00000201586.6:c.423+149T>G ENSP00000201586.1:n.423+149T>G
ENST00000323090.4:c.378+149T>G ENSP00000312880.3:n.378+149T>G
NM_004605.2:c.378+149T>G NP_004596.2:n.378+149T>G
NM_177973.1:c.423+149T>G NP_814444.1:n.423+149T>G
NM_177973.2:c.423+149T>G MANE Select NP_814444.1:n.423+149T>G
Search 100 bp 5'
Search 100 bp 3'