Canonical Allele Identifier: CA365170977

Gene: SOBP

Linked Data

• dbSNP Id: rs747069252
• gnomAD v4: 6-107634541-C-A
• MyVariant Identifiers: chr6:g.107955745C>A (hg19) ; chr6:g.107634541C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634541C>A , CM000668.2:g.107634541C>A	GRCh38
NC_000006.11:g.107955745C>A , CM000668.1:g.107955745C>A	GRCh37
NC_000006.10:g.108062438C>A	NCBI36
NG_028200.1:g.149429C>A
NG_028200.2:g.149429C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1697C>A MANE Select	ENSP00000318900.5:p.Ala566Asp
ENST00000317357.9:c.1697C>A	ENSP00000318900.5:p.Ala566Asp
NM_018013.3:c.1697C>A	NP_060483.3:p.Ala566Asp
XM_005267041.3:c.1850C>A	XP_005267098.1:p.Ala617Asp
XM_005267042.3:c.1754C>A	XP_005267099.1:p.Ala585Asp
XM_011535920.1:c.1850C>A	XP_011534222.1:p.Ala617Asp
XM_011535921.1:c.1736C>A	XP_011534223.1:p.Ala579Asp
XM_011535922.1:c.1109C>A	XP_011534224.1:p.Ala370Asp
XM_011535923.1:c.920C>A	XP_011534225.1:p.Ala307Asp
XM_005267041.4:c.1850C>A	XP_005267098.1:p.Ala617Asp
XM_005267042.4:c.1754C>A	XP_005267099.1:p.Ala585Asp
XM_011535920.2:c.1850C>A	XP_011534222.1:p.Ala617Asp
XM_011535921.2:c.1736C>A	XP_011534223.1:p.Ala579Asp
XM_011535923.2:c.920C>A	XP_011534225.1:p.Ala307Asp
XM_017010991.1:c.1250C>A	XP_016866480.1:p.Ala417Asp
XM_017010992.1:c.1250C>A	XP_016866481.1:p.Ala417Asp
XM_017010993.1:c.1250C>A	XP_016866482.1:p.Ala417Asp
XM_017010994.1:c.1250C>A	XP_016866483.1:p.Ala417Asp
NM_018013.4:c.1697C>A MANE Select	NP_060483.3:p.Ala566Asp