Canonical Allele Identifier: CA365171918

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634933-C-A
• MyVariant Identifiers: chr6:g.107956137C>A (hg19) ; chr6:g.107634933C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634933C>A , CM000668.2:g.107634933C>A	GRCh38
NC_000006.11:g.107956137C>A , CM000668.1:g.107956137C>A	GRCh37
NC_000006.10:g.108062830C>A	NCBI36
NG_028200.1:g.149821C>A
NG_028200.2:g.149821C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.2089C>A MANE Select	ENSP00000318900.5:p.His697Asn
ENST00000317357.9:c.2089C>A	ENSP00000318900.5:p.His697Asn
NM_018013.3:c.2089C>A	NP_060483.3:p.His697Asn
XM_005267041.3:c.2242C>A	XP_005267098.1:p.His748Asn
XM_005267042.3:c.2146C>A	XP_005267099.1:p.His716Asn
XM_011535920.1:c.2242C>A	XP_011534222.1:p.His748Asn
XM_011535921.1:c.2128C>A	XP_011534223.1:p.His710Asn
XM_011535922.1:c.1501C>A	XP_011534224.1:p.His501Asn
XM_011535923.1:c.1312C>A	XP_011534225.1:p.His438Asn
XM_005267041.4:c.2242C>A	XP_005267098.1:p.His748Asn
XM_005267042.4:c.2146C>A	XP_005267099.1:p.His716Asn
XM_011535920.2:c.2242C>A	XP_011534222.1:p.His748Asn
XM_011535921.2:c.2128C>A	XP_011534223.1:p.His710Asn
XM_011535923.2:c.1312C>A	XP_011534225.1:p.His438Asn
XM_017010991.1:c.1642C>A	XP_016866480.1:p.His548Asn
XM_017010992.1:c.1642C>A	XP_016866481.1:p.His548Asn
XM_017010993.1:c.1642C>A	XP_016866482.1:p.His548Asn
XM_017010994.1:c.1642C>A	XP_016866483.1:p.His548Asn
NM_018013.4:c.2089C>A MANE Select	NP_060483.3:p.His697Asn