Canonical Allele Identifier: CA1653939193
Gene: SOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634729A= , CM000668.2:g.107634729A= GRCh38
NC_000006.11:g.107955933A= , CM000668.1:g.107955933A= GRCh37
NC_000006.10:g.108062626A= NCBI36
NG_028200.1:g.149617A=
NG_028200.2:g.149617A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1885A= MANE Select ENSP00000318900.5:p.Ser629=
ENST00000317357.9:c.1885A= ENSP00000318900.5:p.Ser629=
NM_018013.3:c.1885A= NP_060483.3:p.Ser629=
XM_005267041.3:c.2038A= XP_005267098.1:p.Ser680=
XM_005267042.3:c.1942A= XP_005267099.1:p.Ser648=
XM_011535920.1:c.2038A= XP_011534222.1:p.Ser680=
XM_011535921.1:c.1924A= XP_011534223.1:p.Ser642=
XM_011535922.1:c.1297A= XP_011534224.1:p.Ser433=
XM_011535923.1:c.1108A= XP_011534225.1:p.Ser370=
XM_005267041.4:c.2038A= XP_005267098.1:p.Ser680=
XM_005267042.4:c.1942A= XP_005267099.1:p.Ser648=
XM_011535920.2:c.2038A= XP_011534222.1:p.Ser680=
XM_011535921.2:c.1924A= XP_011534223.1:p.Ser642=
XM_011535923.2:c.1108A= XP_011534225.1:p.Ser370=
XM_017010991.1:c.1438A= XP_016866480.1:p.Ser480=
XM_017010992.1:c.1438A= XP_016866481.1:p.Ser480=
XM_017010993.1:c.1438A= XP_016866482.1:p.Ser480=
XM_017010994.1:c.1438A= XP_016866483.1:p.Ser480=
NM_018013.4:c.1885A= MANE Select NP_060483.3:p.Ser629=