Canonical Allele Identifier: CA451581658

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955674T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634470T>G , CM000668.2:g.107634470T>G	GRCh38
NC_000006.11:g.107955674T>G , CM000668.1:g.107955674T>G	GRCh37
NC_000006.10:g.108062367T>G	NCBI36
NG_028200.1:g.149358T>G
NG_028200.2:g.149358T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1626T>G MANE Select	ENSP00000318900.5:p.Pro542=
ENST00000317357.9:c.1626T>G	ENSP00000318900.5:p.Pro542=
NM_018013.3:c.1626T>G	NP_060483.3:p.Pro542=
XM_005267041.3:c.1779T>G	XP_005267098.1:p.Pro593=
XM_005267042.3:c.1683T>G	XP_005267099.1:p.Pro561=
XM_011535920.1:c.1779T>G	XP_011534222.1:p.Pro593=
XM_011535921.1:c.1665T>G	XP_011534223.1:p.Pro555=
XM_011535922.1:c.1038T>G	XP_011534224.1:p.Pro346=
XM_011535923.1:c.849T>G	XP_011534225.1:p.Pro283=
XM_005267041.4:c.1779T>G	XP_005267098.1:p.Pro593=
XM_005267042.4:c.1683T>G	XP_005267099.1:p.Pro561=
XM_011535920.2:c.1779T>G	XP_011534222.1:p.Pro593=
XM_011535921.2:c.1665T>G	XP_011534223.1:p.Pro555=
XM_011535923.2:c.849T>G	XP_011534225.1:p.Pro283=
XM_017010991.1:c.1179T>G	XP_016866480.1:p.Pro393=
XM_017010992.1:c.1179T>G	XP_016866481.1:p.Pro393=
XM_017010993.1:c.1179T>G	XP_016866482.1:p.Pro393=
XM_017010994.1:c.1179T>G	XP_016866483.1:p.Pro393=
NM_018013.4:c.1626T>G MANE Select	NP_060483.3:p.Pro542=