Canonical Allele Identifier: CA451581723

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955701C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634497C>T , CM000668.2:g.107634497C>T	GRCh38
NC_000006.11:g.107955701C>T , CM000668.1:g.107955701C>T	GRCh37
NC_000006.10:g.108062394C>T	NCBI36
NG_028200.1:g.149385C>T
NG_028200.2:g.149385C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1653C>T MANE Select	ENSP00000318900.5:p.Pro551=
ENST00000317357.9:c.1653C>T	ENSP00000318900.5:p.Pro551=
NM_018013.3:c.1653C>T	NP_060483.3:p.Pro551=
XM_005267041.3:c.1806C>T	XP_005267098.1:p.Pro602=
XM_005267042.3:c.1710C>T	XP_005267099.1:p.Pro570=
XM_011535920.1:c.1806C>T	XP_011534222.1:p.Pro602=
XM_011535921.1:c.1692C>T	XP_011534223.1:p.Pro564=
XM_011535922.1:c.1065C>T	XP_011534224.1:p.Pro355=
XM_011535923.1:c.876C>T	XP_011534225.1:p.Pro292=
XM_005267041.4:c.1806C>T	XP_005267098.1:p.Pro602=
XM_005267042.4:c.1710C>T	XP_005267099.1:p.Pro570=
XM_011535920.2:c.1806C>T	XP_011534222.1:p.Pro602=
XM_011535921.2:c.1692C>T	XP_011534223.1:p.Pro564=
XM_011535923.2:c.876C>T	XP_011534225.1:p.Pro292=
XM_017010991.1:c.1206C>T	XP_016866480.1:p.Pro402=
XM_017010992.1:c.1206C>T	XP_016866481.1:p.Pro402=
XM_017010993.1:c.1206C>T	XP_016866482.1:p.Pro402=
XM_017010994.1:c.1206C>T	XP_016866483.1:p.Pro402=
NM_018013.4:c.1653C>T MANE Select	NP_060483.3:p.Pro551=