Canonical Allele Identifier: CA365171901

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634926-G-T
• MyVariant Identifiers: chr6:g.107956130G>T (hg19) ; chr6:g.107634926G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634926G>T , CM000668.2:g.107634926G>T	GRCh38
NC_000006.11:g.107956130G>T , CM000668.1:g.107956130G>T	GRCh37
NC_000006.10:g.108062823G>T	NCBI36
NG_028200.1:g.149814G>T
NG_028200.2:g.149814G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.2082G>T MANE Select	ENSP00000318900.5:p.Arg694Ser
ENST00000317357.9:c.2082G>T	ENSP00000318900.5:p.Arg694Ser
NM_018013.3:c.2082G>T	NP_060483.3:p.Arg694Ser
XM_005267041.3:c.2235G>T	XP_005267098.1:p.Arg745Ser
XM_005267042.3:c.2139G>T	XP_005267099.1:p.Arg713Ser
XM_011535920.1:c.2235G>T	XP_011534222.1:p.Arg745Ser
XM_011535921.1:c.2121G>T	XP_011534223.1:p.Arg707Ser
XM_011535922.1:c.1494G>T	XP_011534224.1:p.Arg498Ser
XM_011535923.1:c.1305G>T	XP_011534225.1:p.Arg435Ser
XM_005267041.4:c.2235G>T	XP_005267098.1:p.Arg745Ser
XM_005267042.4:c.2139G>T	XP_005267099.1:p.Arg713Ser
XM_011535920.2:c.2235G>T	XP_011534222.1:p.Arg745Ser
XM_011535921.2:c.2121G>T	XP_011534223.1:p.Arg707Ser
XM_011535923.2:c.1305G>T	XP_011534225.1:p.Arg435Ser
XM_017010991.1:c.1635G>T	XP_016866480.1:p.Arg545Ser
XM_017010992.1:c.1635G>T	XP_016866481.1:p.Arg545Ser
XM_017010993.1:c.1635G>T	XP_016866482.1:p.Arg545Ser
XM_017010994.1:c.1635G>T	XP_016866483.1:p.Arg545Ser
NM_018013.4:c.2082G>T MANE Select	NP_060483.3:p.Arg694Ser