Canonical Allele Identifier: CA451581813

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955749T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634545T>A , CM000668.2:g.107634545T>A	GRCh38
NC_000006.11:g.107955749T>A , CM000668.1:g.107955749T>A	GRCh37
NC_000006.10:g.108062442T>A	NCBI36
NG_028200.1:g.149433T>A
NG_028200.2:g.149433T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1701T>A MANE Select	ENSP00000318900.5:p.Pro567=
ENST00000317357.9:c.1701T>A	ENSP00000318900.5:p.Pro567=
NM_018013.3:c.1701T>A	NP_060483.3:p.Pro567=
XM_005267041.3:c.1854T>A	XP_005267098.1:p.Pro618=
XM_005267042.3:c.1758T>A	XP_005267099.1:p.Pro586=
XM_011535920.1:c.1854T>A	XP_011534222.1:p.Pro618=
XM_011535921.1:c.1740T>A	XP_011534223.1:p.Pro580=
XM_011535922.1:c.1113T>A	XP_011534224.1:p.Pro371=
XM_011535923.1:c.924T>A	XP_011534225.1:p.Pro308=
XM_005267041.4:c.1854T>A	XP_005267098.1:p.Pro618=
XM_005267042.4:c.1758T>A	XP_005267099.1:p.Pro586=
XM_011535920.2:c.1854T>A	XP_011534222.1:p.Pro618=
XM_011535921.2:c.1740T>A	XP_011534223.1:p.Pro580=
XM_011535923.2:c.924T>A	XP_011534225.1:p.Pro308=
XM_017010991.1:c.1254T>A	XP_016866480.1:p.Pro418=
XM_017010992.1:c.1254T>A	XP_016866481.1:p.Pro418=
XM_017010993.1:c.1254T>A	XP_016866482.1:p.Pro418=
XM_017010994.1:c.1254T>A	XP_016866483.1:p.Pro418=
NM_018013.4:c.1701T>A MANE Select	NP_060483.3:p.Pro567=