Canonical Allele Identifier: CA2258597277
Gene: SOCS7 HGNC NCBI

Linked Data

dbSNP Id: rs12051836
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.38393251T>G , CM000679.2:g.38393251T>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000612932.6:c.1682-2058T>G MANE Select ENSP00000482229.2:n.1682-2058T>G
ENST00000613678.5:c.1405-2058T>G
ENST00000665913.1:c.1490-2058T>G ENSP00000499750.1:n.1490-2058T>G
ENST00000612932.4:c.1490-2058T>G ENSP00000482229.1:n.1490-2058T>G
ENST00000613678.4:c.1388-2058T>G ENSP00000484381.1:n.1388-2058T>G
ENST00000617360.1:n.1931-6262T>G
NM_014598.3:c.1490-2058T>G NP_055413.1:n.1490-2058T>G
XM_017024551.1:c.1580-2058T>G XP_016880040.1:n.1580-2058T>G
XM_017024552.1:c.1475-2058T>G XP_016880041.1:n.1475-2058T>G
XR_001752503.1:n.2051-2058T>G
NM_014598.4:c.1682-2058T>G MANE Select NP_055413.2:n.1682-2058T>G
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