Canonical Allele Identifier: CA508042765
Gene: SULT2B1 HGNC NCBI

Linked Data

dbSNP Id: rs1163038527
gnomAD v2: 19-49090643-C-G
gnomAD v3: 19-48587386-C-G
gnomAD v4: 19-48587386-C-G
MyVariant Identifiers: chr19:g.49090643C>G (hg19) chr19:g.48587386C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48587386C>G , CM000681.2:g.48587386C>G GRCh38
NC_000019.9:g.49090643C>G , CM000681.1:g.49090643C>G GRCh37
NC_000019.8:g.53782455C>G NCBI36
NG_029063.1:g.40215C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000201586.7:c.372C>G MANE Select ENSP00000201586.2:p.Ser124=
ENST00000201586.6:c.372C>G ENSP00000201586.1:p.Ser124=
ENST00000323090.4:c.327C>G ENSP00000312880.3:p.Ser109=
NM_004605.2:c.327C>G NP_004596.2:p.Ser109=
NM_177973.1:c.372C>G NP_814444.1:p.Ser124=
NM_177973.2:c.372C>G MANE Select NP_814444.1:p.Ser124=
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