Canonical Allele Identifier: CA451581897
Gene: SOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.107955776G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634572G>A , CM000668.2:g.107634572G>A GRCh38
NC_000006.11:g.107955776G>A , CM000668.1:g.107955776G>A GRCh37
NC_000006.10:g.108062469G>A NCBI36
NG_028200.1:g.149460G>A
NG_028200.2:g.149460G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1728G>A MANE Select ENSP00000318900.5:p.Lys576=
ENST00000317357.9:c.1728G>A ENSP00000318900.5:p.Lys576=
NM_018013.3:c.1728G>A NP_060483.3:p.Lys576=
XM_005267041.3:c.1881G>A XP_005267098.1:p.Lys627=
XM_005267042.3:c.1785G>A XP_005267099.1:p.Lys595=
XM_011535920.1:c.1881G>A XP_011534222.1:p.Lys627=
XM_011535921.1:c.1767G>A XP_011534223.1:p.Lys589=
XM_011535922.1:c.1140G>A XP_011534224.1:p.Lys380=
XM_011535923.1:c.951G>A XP_011534225.1:p.Lys317=
XM_005267041.4:c.1881G>A XP_005267098.1:p.Lys627=
XM_005267042.4:c.1785G>A XP_005267099.1:p.Lys595=
XM_011535920.2:c.1881G>A XP_011534222.1:p.Lys627=
XM_011535921.2:c.1767G>A XP_011534223.1:p.Lys589=
XM_011535923.2:c.951G>A XP_011534225.1:p.Lys317=
XM_017010991.1:c.1281G>A XP_016866480.1:p.Lys427=
XM_017010992.1:c.1281G>A XP_016866481.1:p.Lys427=
XM_017010993.1:c.1281G>A XP_016866482.1:p.Lys427=
XM_017010994.1:c.1281G>A XP_016866483.1:p.Lys427=
NM_018013.4:c.1728G>A MANE Select NP_060483.3:p.Lys576=