Canonical Allele Identifier: CA365170805
Gene: SOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634511C>A , CM000668.2:g.107634511C>A GRCh38
NC_000006.11:g.107955715C>A , CM000668.1:g.107955715C>A GRCh37
NC_000006.10:g.108062408C>A NCBI36
NG_028200.1:g.149399C>A
NG_028200.2:g.149399C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1667C>A MANE Select ENSP00000318900.5:p.Ser556Tyr
ENST00000317357.9:c.1667C>A ENSP00000318900.5:p.Ser556Tyr
NM_018013.3:c.1667C>A NP_060483.3:p.Ser556Tyr
XM_005267041.3:c.1820C>A XP_005267098.1:p.Ser607Tyr
XM_005267042.3:c.1724C>A XP_005267099.1:p.Ser575Tyr
XM_011535920.1:c.1820C>A XP_011534222.1:p.Ser607Tyr
XM_011535921.1:c.1706C>A XP_011534223.1:p.Ser569Tyr
XM_011535922.1:c.1079C>A XP_011534224.1:p.Ser360Tyr
XM_011535923.1:c.890C>A XP_011534225.1:p.Ser297Tyr
XM_005267041.4:c.1820C>A XP_005267098.1:p.Ser607Tyr
XM_005267042.4:c.1724C>A XP_005267099.1:p.Ser575Tyr
XM_011535920.2:c.1820C>A XP_011534222.1:p.Ser607Tyr
XM_011535921.2:c.1706C>A XP_011534223.1:p.Ser569Tyr
XM_011535923.2:c.890C>A XP_011534225.1:p.Ser297Tyr
XM_017010991.1:c.1220C>A XP_016866480.1:p.Ser407Tyr
XM_017010992.1:c.1220C>A XP_016866481.1:p.Ser407Tyr
XM_017010993.1:c.1220C>A XP_016866482.1:p.Ser407Tyr
XM_017010994.1:c.1220C>A XP_016866483.1:p.Ser407Tyr
NM_018013.4:c.1667C>A MANE Select NP_060483.3:p.Ser556Tyr