Canonical Allele Identifier: CA365171265

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634619-C-G
• MyVariant Identifiers: chr6:g.107955823C>G (hg19) ; chr6:g.107634619C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634619C>G , CM000668.2:g.107634619C>G	GRCh38
NC_000006.11:g.107955823C>G , CM000668.1:g.107955823C>G	GRCh37
NC_000006.10:g.108062516C>G	NCBI36
NG_028200.1:g.149507C>G
NG_028200.2:g.149507C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1775C>G MANE Select	ENSP00000318900.5:p.Ser592Cys
ENST00000317357.9:c.1775C>G	ENSP00000318900.5:p.Ser592Cys
NM_018013.3:c.1775C>G	NP_060483.3:p.Ser592Cys
XM_005267041.3:c.1928C>G	XP_005267098.1:p.Ser643Cys
XM_005267042.3:c.1832C>G	XP_005267099.1:p.Ser611Cys
XM_011535920.1:c.1928C>G	XP_011534222.1:p.Ser643Cys
XM_011535921.1:c.1814C>G	XP_011534223.1:p.Ser605Cys
XM_011535922.1:c.1187C>G	XP_011534224.1:p.Ser396Cys
XM_011535923.1:c.998C>G	XP_011534225.1:p.Ser333Cys
XM_005267041.4:c.1928C>G	XP_005267098.1:p.Ser643Cys
XM_005267042.4:c.1832C>G	XP_005267099.1:p.Ser611Cys
XM_011535920.2:c.1928C>G	XP_011534222.1:p.Ser643Cys
XM_011535921.2:c.1814C>G	XP_011534223.1:p.Ser605Cys
XM_011535923.2:c.998C>G	XP_011534225.1:p.Ser333Cys
XM_017010991.1:c.1328C>G	XP_016866480.1:p.Ser443Cys
XM_017010992.1:c.1328C>G	XP_016866481.1:p.Ser443Cys
XM_017010993.1:c.1328C>G	XP_016866482.1:p.Ser443Cys
XM_017010994.1:c.1328C>G	XP_016866483.1:p.Ser443Cys
NM_018013.4:c.1775C>G MANE Select	NP_060483.3:p.Ser592Cys