Canonical Allele Identifier: CA294359293

Gene: SOCS3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78357871C>T , CM000679.2:g.78357871C>T	GRCh38
NC_000017.10:g.76353952C>T , CM000679.1:g.76353952C>T	GRCh37
NC_000017.9:g.73865547C>T	NCBI36
NG_016851.1:g.7207G>A , LRG_619:g.7207G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330871.3:c.*547G>A MANE Select	ENSP00000330341.2:n.*547G>A
NM_003955.4:c.*547G>A , LRG_619t1:c.*547G>A	NP_003946.3:n.*547G>A
NM_001378932.1:c.*547G>A	NP_001365861.1:n.*547G>A
NM_001378933.1:c.*547G>A	NP_001365862.1:n.*547G>A
NM_003955.5:c.*547G>A MANE Select	NP_003946.3:n.*547G>A