Canonical Allele Identifier: CA451581653

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634725-C-G
• MyVariant Identifiers: chr6:g.107955929C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634725C>G , CM000668.2:g.107634725C>G	GRCh38
NC_000006.11:g.107955929C>G , CM000668.1:g.107955929C>G	GRCh37
NC_000006.10:g.108062622C>G	NCBI36
NG_028200.1:g.149613C>G
NG_028200.2:g.149613C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1881C>G MANE Select	ENSP00000318900.5:p.Ala627=
ENST00000317357.9:c.1881C>G	ENSP00000318900.5:p.Ala627=
NM_018013.3:c.1881C>G	NP_060483.3:p.Ala627=
XM_005267041.3:c.2034C>G	XP_005267098.1:p.Ala678=
XM_005267042.3:c.1938C>G	XP_005267099.1:p.Ala646=
XM_011535920.1:c.2034C>G	XP_011534222.1:p.Ala678=
XM_011535921.1:c.1920C>G	XP_011534223.1:p.Ala640=
XM_011535922.1:c.1293C>G	XP_011534224.1:p.Ala431=
XM_011535923.1:c.1104C>G	XP_011534225.1:p.Ala368=
XM_005267041.4:c.2034C>G	XP_005267098.1:p.Ala678=
XM_005267042.4:c.1938C>G	XP_005267099.1:p.Ala646=
XM_011535920.2:c.2034C>G	XP_011534222.1:p.Ala678=
XM_011535921.2:c.1920C>G	XP_011534223.1:p.Ala640=
XM_011535923.2:c.1104C>G	XP_011534225.1:p.Ala368=
XM_017010991.1:c.1434C>G	XP_016866480.1:p.Ala478=
XM_017010992.1:c.1434C>G	XP_016866481.1:p.Ala478=
XM_017010993.1:c.1434C>G	XP_016866482.1:p.Ala478=
XM_017010994.1:c.1434C>G	XP_016866483.1:p.Ala478=
NM_018013.4:c.1881C>G MANE Select	NP_060483.3:p.Ala627=