Canonical Allele Identifier: CA365171333

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634652-G-T
• MyVariant Identifiers: chr6:g.107955856G>T (hg19) ; chr6:g.107634652G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634652G>T , CM000668.2:g.107634652G>T	GRCh38
NC_000006.11:g.107955856G>T , CM000668.1:g.107955856G>T	GRCh37
NC_000006.10:g.108062549G>T	NCBI36
NG_028200.1:g.149540G>T
NG_028200.2:g.149540G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1808G>T MANE Select	ENSP00000318900.5:p.Gly603Val
ENST00000317357.9:c.1808G>T	ENSP00000318900.5:p.Gly603Val
NM_018013.3:c.1808G>T	NP_060483.3:p.Gly603Val
XM_005267041.3:c.1961G>T	XP_005267098.1:p.Gly654Val
XM_005267042.3:c.1865G>T	XP_005267099.1:p.Gly622Val
XM_011535920.1:c.1961G>T	XP_011534222.1:p.Gly654Val
XM_011535921.1:c.1847G>T	XP_011534223.1:p.Gly616Val
XM_011535922.1:c.1220G>T	XP_011534224.1:p.Gly407Val
XM_011535923.1:c.1031G>T	XP_011534225.1:p.Gly344Val
XM_005267041.4:c.1961G>T	XP_005267098.1:p.Gly654Val
XM_005267042.4:c.1865G>T	XP_005267099.1:p.Gly622Val
XM_011535920.2:c.1961G>T	XP_011534222.1:p.Gly654Val
XM_011535921.2:c.1847G>T	XP_011534223.1:p.Gly616Val
XM_011535923.2:c.1031G>T	XP_011534225.1:p.Gly344Val
XM_017010991.1:c.1361G>T	XP_016866480.1:p.Gly454Val
XM_017010992.1:c.1361G>T	XP_016866481.1:p.Gly454Val
XM_017010993.1:c.1361G>T	XP_016866482.1:p.Gly454Val
XM_017010994.1:c.1361G>T	XP_016866483.1:p.Gly454Val
NM_018013.4:c.1808G>T MANE Select	NP_060483.3:p.Gly603Val