Canonical Allele Identifier: CA145013439

Gene: SOBP

Linked Data

• dbSNP Id: rs376863861
• gnomAD v2: 6-107955683-C-A
• gnomAD v4: 6-107634479-C-A
• MyVariant Identifiers: chr6:g.107955683C>A (hg19) ; chr6:g.107634479C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634479C>A , CM000668.2:g.107634479C>A	GRCh38
NC_000006.11:g.107955683C>A , CM000668.1:g.107955683C>A	GRCh37
NC_000006.10:g.108062376C>A	NCBI36
NG_028200.1:g.149367C>A
NG_028200.2:g.149367C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1635C>A MANE Select	ENSP00000318900.5:p.His545Gln
ENST00000317357.9:c.1635C>A	ENSP00000318900.5:p.His545Gln
NM_018013.3:c.1635C>A	NP_060483.3:p.His545Gln
XM_005267041.3:c.1788C>A	XP_005267098.1:p.His596Gln
XM_005267042.3:c.1692C>A	XP_005267099.1:p.His564Gln
XM_011535920.1:c.1788C>A	XP_011534222.1:p.His596Gln
XM_011535921.1:c.1674C>A	XP_011534223.1:p.His558Gln
XM_011535922.1:c.1047C>A	XP_011534224.1:p.His349Gln
XM_011535923.1:c.858C>A	XP_011534225.1:p.His286Gln
XM_005267041.4:c.1788C>A	XP_005267098.1:p.His596Gln
XM_005267042.4:c.1692C>A	XP_005267099.1:p.His564Gln
XM_011535920.2:c.1788C>A	XP_011534222.1:p.His596Gln
XM_011535921.2:c.1674C>A	XP_011534223.1:p.His558Gln
XM_011535923.2:c.858C>A	XP_011534225.1:p.His286Gln
XM_017010991.1:c.1188C>A	XP_016866480.1:p.His396Gln
XM_017010992.1:c.1188C>A	XP_016866481.1:p.His396Gln
XM_017010993.1:c.1188C>A	XP_016866482.1:p.His396Gln
XM_017010994.1:c.1188C>A	XP_016866483.1:p.His396Gln
NM_018013.4:c.1635C>A MANE Select	NP_060483.3:p.His545Gln