Canonical Allele Identifier: CA1653939211
Gene: SOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634734C= , CM000668.2:g.107634734C= GRCh38
NC_000006.11:g.107955938C= , CM000668.1:g.107955938C= GRCh37
NC_000006.10:g.108062631C= NCBI36
NG_028200.1:g.149622C=
NG_028200.2:g.149622C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1890C= MANE Select ENSP00000318900.5:p.Pro630=
ENST00000317357.9:c.1890C= ENSP00000318900.5:p.Pro630=
NM_018013.3:c.1890C= NP_060483.3:p.Pro630=
XM_005267041.3:c.2043C= XP_005267098.1:p.Pro681=
XM_005267042.3:c.1947C= XP_005267099.1:p.Pro649=
XM_011535920.1:c.2043C= XP_011534222.1:p.Pro681=
XM_011535921.1:c.1929C= XP_011534223.1:p.Pro643=
XM_011535922.1:c.1302C= XP_011534224.1:p.Pro434=
XM_011535923.1:c.1113C= XP_011534225.1:p.Pro371=
XM_005267041.4:c.2043C= XP_005267098.1:p.Pro681=
XM_005267042.4:c.1947C= XP_005267099.1:p.Pro649=
XM_011535920.2:c.2043C= XP_011534222.1:p.Pro681=
XM_011535921.2:c.1929C= XP_011534223.1:p.Pro643=
XM_011535923.2:c.1113C= XP_011534225.1:p.Pro371=
XM_017010991.1:c.1443C= XP_016866480.1:p.Pro481=
XM_017010992.1:c.1443C= XP_016866481.1:p.Pro481=
XM_017010993.1:c.1443C= XP_016866482.1:p.Pro481=
XM_017010994.1:c.1443C= XP_016866483.1:p.Pro481=
NM_018013.4:c.1890C= MANE Select NP_060483.3:p.Pro630=