Canonical Allele Identifier: CA365171686

Gene: SOBP

Linked Data

• dbSNP Id: rs1473974100
• gnomAD v2: 6-107956033-C-T
• gnomAD v4: 6-107634829-C-T
• MyVariant Identifiers: chr6:g.107956033C>T (hg19) ; chr6:g.107634829C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634829C>T , CM000668.2:g.107634829C>T	GRCh38
NC_000006.11:g.107956033C>T , CM000668.1:g.107956033C>T	GRCh37
NC_000006.10:g.108062726C>T	NCBI36
NG_028200.1:g.149717C>T
NG_028200.2:g.149717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1985C>T MANE Select	ENSP00000318900.5:p.Ala662Val
ENST00000317357.9:c.1985C>T	ENSP00000318900.5:p.Ala662Val
NM_018013.3:c.1985C>T	NP_060483.3:p.Ala662Val
XM_005267041.3:c.2138C>T	XP_005267098.1:p.Ala713Val
XM_005267042.3:c.2042C>T	XP_005267099.1:p.Ala681Val
XM_011535920.1:c.2138C>T	XP_011534222.1:p.Ala713Val
XM_011535921.1:c.2024C>T	XP_011534223.1:p.Ala675Val
XM_011535922.1:c.1397C>T	XP_011534224.1:p.Ala466Val
XM_011535923.1:c.1208C>T	XP_011534225.1:p.Ala403Val
XM_005267041.4:c.2138C>T	XP_005267098.1:p.Ala713Val
XM_005267042.4:c.2042C>T	XP_005267099.1:p.Ala681Val
XM_011535920.2:c.2138C>T	XP_011534222.1:p.Ala713Val
XM_011535921.2:c.2024C>T	XP_011534223.1:p.Ala675Val
XM_011535923.2:c.1208C>T	XP_011534225.1:p.Ala403Val
XM_017010991.1:c.1538C>T	XP_016866480.1:p.Ala513Val
XM_017010992.1:c.1538C>T	XP_016866481.1:p.Ala513Val
XM_017010993.1:c.1538C>T	XP_016866482.1:p.Ala513Val
XM_017010994.1:c.1538C>T	XP_016866483.1:p.Ala513Val
NM_018013.4:c.1985C>T MANE Select	NP_060483.3:p.Ala662Val