Canonical Allele Identifier: CA633602056
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs1258550774
gnomAD v2: 19-49090923-A-C
gnomAD v3: 19-48587666-A-C
gnomAD v4: 19-48587666-A-C
MyVariant Identifiers: chr19:g.49090923A>C (hg19) chr19:g.48587666A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587666A>C , CM000681.2:g.48587666A>C GRCh38
NC_000019.9:g.49090923A>C , CM000681.1:g.49090923A>C GRCh37
NC_000019.8:g.53782735A>C NCBI36
NG_029063.1:g.40495A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.423+229A>C MANE Select ENSP00000201586.2:n.423+229A>C
ENST00000201586.6:c.423+229A>C ENSP00000201586.1:n.423+229A>C
ENST00000323090.4:c.378+229A>C ENSP00000312880.3:n.378+229A>C
NM_004605.2:c.378+229A>C NP_004596.2:n.378+229A>C
NM_177973.1:c.423+229A>C NP_814444.1:n.423+229A>C
NM_177973.2:c.423+229A>C MANE Select NP_814444.1:n.423+229A>C
Search 100 bp 5'
Search 100 bp 3'