Canonical Allele Identifier: CA726248705
Gene: HS3ST3A1 HGNC NCBI

Linked Data

dbSNP Id: rs1290421870
gnomAD v3: 17-13573778-G-C
gnomAD v4: 17-13573778-G-C
MyVariant Identifiers: chr17:g.13477095G>C (hg19) chr17:g.13573778G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.13573778G>C , CM000679.2:g.13573778G>C GRCh38
NC_000017.10:g.13477095G>C , CM000679.1:g.13477095G>C GRCh37
NC_000017.9:g.13417820G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000284110.2:c.599+26753C>G MANE Select ENSP00000284110.1:n.599+26753C>G
ENST00000284110.1:c.599+26753C>G ENSP00000284110.1:n.599+26753C>G
NM_006042.2:c.599+26753C>G NP_006033.1:n.599+26753C>G
NM_006042.3:c.599+26753C>G MANE Select NP_006033.1:n.599+26753C>G
Search 100 bp 5'
Search 100 bp 3'