Canonical Allele Identifier: CA365171851

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634904-G-C
• MyVariant Identifiers: chr6:g.107956108G>C (hg19) ; chr6:g.107634904G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634904G>C , CM000668.2:g.107634904G>C	GRCh38
NC_000006.11:g.107956108G>C , CM000668.1:g.107956108G>C	GRCh37
NC_000006.10:g.108062801G>C	NCBI36
NG_028200.1:g.149792G>C
NG_028200.2:g.149792G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.2060G>C MANE Select	ENSP00000318900.5:p.Arg687Pro
ENST00000317357.9:c.2060G>C	ENSP00000318900.5:p.Arg687Pro
NM_018013.3:c.2060G>C	NP_060483.3:p.Arg687Pro
XM_005267041.3:c.2213G>C	XP_005267098.1:p.Arg738Pro
XM_005267042.3:c.2117G>C	XP_005267099.1:p.Arg706Pro
XM_011535920.1:c.2213G>C	XP_011534222.1:p.Arg738Pro
XM_011535921.1:c.2099G>C	XP_011534223.1:p.Arg700Pro
XM_011535922.1:c.1472G>C	XP_011534224.1:p.Arg491Pro
XM_011535923.1:c.1283G>C	XP_011534225.1:p.Arg428Pro
XM_005267041.4:c.2213G>C	XP_005267098.1:p.Arg738Pro
XM_005267042.4:c.2117G>C	XP_005267099.1:p.Arg706Pro
XM_011535920.2:c.2213G>C	XP_011534222.1:p.Arg738Pro
XM_011535921.2:c.2099G>C	XP_011534223.1:p.Arg700Pro
XM_011535923.2:c.1283G>C	XP_011534225.1:p.Arg428Pro
XM_017010991.1:c.1613G>C	XP_016866480.1:p.Arg538Pro
XM_017010992.1:c.1613G>C	XP_016866481.1:p.Arg538Pro
XM_017010993.1:c.1613G>C	XP_016866482.1:p.Arg538Pro
XM_017010994.1:c.1613G>C	XP_016866483.1:p.Arg538Pro
NM_018013.4:c.2060G>C MANE Select	NP_060483.3:p.Arg687Pro