Canonical Allele Identifier: CA365171337

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955859A>G (hg19) ; chr6:g.107634655A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634655A>G , CM000668.2:g.107634655A>G	GRCh38
NC_000006.11:g.107955859A>G , CM000668.1:g.107955859A>G	GRCh37
NC_000006.10:g.108062552A>G	NCBI36
NG_028200.1:g.149543A>G
NG_028200.2:g.149543A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1811A>G MANE Select	ENSP00000318900.5:p.Gln604Arg
ENST00000317357.9:c.1811A>G	ENSP00000318900.5:p.Gln604Arg
NM_018013.3:c.1811A>G	NP_060483.3:p.Gln604Arg
XM_005267041.3:c.1964A>G	XP_005267098.1:p.Gln655Arg
XM_005267042.3:c.1868A>G	XP_005267099.1:p.Gln623Arg
XM_011535920.1:c.1964A>G	XP_011534222.1:p.Gln655Arg
XM_011535921.1:c.1850A>G	XP_011534223.1:p.Gln617Arg
XM_011535922.1:c.1223A>G	XP_011534224.1:p.Gln408Arg
XM_011535923.1:c.1034A>G	XP_011534225.1:p.Gln345Arg
XM_005267041.4:c.1964A>G	XP_005267098.1:p.Gln655Arg
XM_005267042.4:c.1868A>G	XP_005267099.1:p.Gln623Arg
XM_011535920.2:c.1964A>G	XP_011534222.1:p.Gln655Arg
XM_011535921.2:c.1850A>G	XP_011534223.1:p.Gln617Arg
XM_011535923.2:c.1034A>G	XP_011534225.1:p.Gln345Arg
XM_017010991.1:c.1364A>G	XP_016866480.1:p.Gln455Arg
XM_017010992.1:c.1364A>G	XP_016866481.1:p.Gln455Arg
XM_017010993.1:c.1364A>G	XP_016866482.1:p.Gln455Arg
XM_017010994.1:c.1364A>G	XP_016866483.1:p.Gln455Arg
NM_018013.4:c.1811A>G MANE Select	NP_060483.3:p.Gln604Arg