Canonical Allele Identifier: CA365171340

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955860G>T (hg19) ; chr6:g.107634656G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634656G>T , CM000668.2:g.107634656G>T	GRCh38
NC_000006.11:g.107955860G>T , CM000668.1:g.107955860G>T	GRCh37
NC_000006.10:g.108062553G>T	NCBI36
NG_028200.1:g.149544G>T
NG_028200.2:g.149544G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1812G>T MANE Select	ENSP00000318900.5:p.Gln604His
ENST00000317357.9:c.1812G>T	ENSP00000318900.5:p.Gln604His
NM_018013.3:c.1812G>T	NP_060483.3:p.Gln604His
XM_005267041.3:c.1965G>T	XP_005267098.1:p.Gln655His
XM_005267042.3:c.1869G>T	XP_005267099.1:p.Gln623His
XM_011535920.1:c.1965G>T	XP_011534222.1:p.Gln655His
XM_011535921.1:c.1851G>T	XP_011534223.1:p.Gln617His
XM_011535922.1:c.1224G>T	XP_011534224.1:p.Gln408His
XM_011535923.1:c.1035G>T	XP_011534225.1:p.Gln345His
XM_005267041.4:c.1965G>T	XP_005267098.1:p.Gln655His
XM_005267042.4:c.1869G>T	XP_005267099.1:p.Gln623His
XM_011535920.2:c.1965G>T	XP_011534222.1:p.Gln655His
XM_011535921.2:c.1851G>T	XP_011534223.1:p.Gln617His
XM_011535923.2:c.1035G>T	XP_011534225.1:p.Gln345His
XM_017010991.1:c.1365G>T	XP_016866480.1:p.Gln455His
XM_017010992.1:c.1365G>T	XP_016866481.1:p.Gln455His
XM_017010993.1:c.1365G>T	XP_016866482.1:p.Gln455His
XM_017010994.1:c.1365G>T	XP_016866483.1:p.Gln455His
NM_018013.4:c.1812G>T MANE Select	NP_060483.3:p.Gln604His