Canonical Allele Identifier: CA365170782

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955711T>G (hg19) ; chr6:g.107634507T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634507T>G , CM000668.2:g.107634507T>G	GRCh38
NC_000006.11:g.107955711T>G , CM000668.1:g.107955711T>G	GRCh37
NC_000006.10:g.108062404T>G	NCBI36
NG_028200.1:g.149395T>G
NG_028200.2:g.149395T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1663T>G MANE Select	ENSP00000318900.5:p.Phe555Val
ENST00000317357.9:c.1663T>G	ENSP00000318900.5:p.Phe555Val
NM_018013.3:c.1663T>G	NP_060483.3:p.Phe555Val
XM_005267041.3:c.1816T>G	XP_005267098.1:p.Phe606Val
XM_005267042.3:c.1720T>G	XP_005267099.1:p.Phe574Val
XM_011535920.1:c.1816T>G	XP_011534222.1:p.Phe606Val
XM_011535921.1:c.1702T>G	XP_011534223.1:p.Phe568Val
XM_011535922.1:c.1075T>G	XP_011534224.1:p.Phe359Val
XM_011535923.1:c.886T>G	XP_011534225.1:p.Phe296Val
XM_005267041.4:c.1816T>G	XP_005267098.1:p.Phe606Val
XM_005267042.4:c.1720T>G	XP_005267099.1:p.Phe574Val
XM_011535920.2:c.1816T>G	XP_011534222.1:p.Phe606Val
XM_011535921.2:c.1702T>G	XP_011534223.1:p.Phe568Val
XM_011535923.2:c.886T>G	XP_011534225.1:p.Phe296Val
XM_017010991.1:c.1216T>G	XP_016866480.1:p.Phe406Val
XM_017010992.1:c.1216T>G	XP_016866481.1:p.Phe406Val
XM_017010993.1:c.1216T>G	XP_016866482.1:p.Phe406Val
XM_017010994.1:c.1216T>G	XP_016866483.1:p.Phe406Val
NM_018013.4:c.1663T>G MANE Select	NP_060483.3:p.Phe555Val