Canonical Allele Identifier: CA68773968
Gene: SUMF1 HGNC NCBI

Linked Data

dbSNP Id: rs559950746
MyVariant Identifiers: chr3:g.4376076T>G (hg19) chr3:g.4334392T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4334392T>G , CM000665.2:g.4334392T>G GRCh38
NC_000003.11:g.4376076T>G , CM000665.1:g.4376076T>G GRCh37
NC_000003.10:g.4351076T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000448413.5:c.1014+41938A>C ENSP00000404384.1:n.1014+41938A>C
XM_011533623.1:c.1014+41938A>C XP_011531925.1:n.1014+41938A>C
XM_011533624.1:c.1014+41938A>C XP_011531926.1:n.1014+41938A>C
XM_011533625.1:c.1015-29790A>C XP_011531927.1:n.1015-29790A>C
XM_011533624.3:c.1014+41938A>C XP_011531926.1:n.1014+41938A>C
XM_011533625.3:c.1015-29790A>C XP_011531927.1:n.1015-29790A>C
XM_017006252.2:c.954+76473A>C XP_016861741.1:n.954+76473A>C
XM_017006253.1:c.939+41938A>C XP_016861742.1:n.939+41938A>C
XM_017006254.2:c.1014+41938A>C XP_016861743.1:n.1014+41938A>C
XM_017006255.2:c.1015-22889A>C XP_016861744.1:n.1015-22889A>C
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