Canonical Allele Identifier: CA365171684

Gene: SOBP

Linked Data

• dbSNP Id: rs1412463552
• gnomAD v3: 6-107634828-G-C
• gnomAD v4: 6-107634828-G-C
• MyVariant Identifiers: chr6:g.107956032G>C (hg19) ; chr6:g.107634828G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634828G>C , CM000668.2:g.107634828G>C	GRCh38
NC_000006.11:g.107956032G>C , CM000668.1:g.107956032G>C	GRCh37
NC_000006.10:g.108062725G>C	NCBI36
NG_028200.1:g.149716G>C
NG_028200.2:g.149716G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1984G>C MANE Select	ENSP00000318900.5:p.Ala662Pro
ENST00000317357.9:c.1984G>C	ENSP00000318900.5:p.Ala662Pro
NM_018013.3:c.1984G>C	NP_060483.3:p.Ala662Pro
XM_005267041.3:c.2137G>C	XP_005267098.1:p.Ala713Pro
XM_005267042.3:c.2041G>C	XP_005267099.1:p.Ala681Pro
XM_011535920.1:c.2137G>C	XP_011534222.1:p.Ala713Pro
XM_011535921.1:c.2023G>C	XP_011534223.1:p.Ala675Pro
XM_011535922.1:c.1396G>C	XP_011534224.1:p.Ala466Pro
XM_011535923.1:c.1207G>C	XP_011534225.1:p.Ala403Pro
XM_005267041.4:c.2137G>C	XP_005267098.1:p.Ala713Pro
XM_005267042.4:c.2041G>C	XP_005267099.1:p.Ala681Pro
XM_011535920.2:c.2137G>C	XP_011534222.1:p.Ala713Pro
XM_011535921.2:c.2023G>C	XP_011534223.1:p.Ala675Pro
XM_011535923.2:c.1207G>C	XP_011534225.1:p.Ala403Pro
XM_017010991.1:c.1537G>C	XP_016866480.1:p.Ala513Pro
XM_017010992.1:c.1537G>C	XP_016866481.1:p.Ala513Pro
XM_017010993.1:c.1537G>C	XP_016866482.1:p.Ala513Pro
XM_017010994.1:c.1537G>C	XP_016866483.1:p.Ala513Pro
NM_018013.4:c.1984G>C MANE Select	NP_060483.3:p.Ala662Pro