Canonical Allele Identifier: CA365170389
Gene: SOBP HGNC NCBI

Linked Data

dbSNP Id: rs1306190535

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634462C>A , CM000668.2:g.107634462C>A GRCh38
NC_000006.11:g.107955666C>A , CM000668.1:g.107955666C>A GRCh37
NC_000006.10:g.108062359C>A NCBI36
NG_028200.1:g.149350C>A
NG_028200.2:g.149350C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1618C>A MANE Select ENSP00000318900.5:p.Pro540Thr
ENST00000317357.9:c.1618C>A ENSP00000318900.5:p.Pro540Thr
NM_018013.3:c.1618C>A NP_060483.3:p.Pro540Thr
XM_005267041.3:c.1771C>A XP_005267098.1:p.Pro591Thr
XM_005267042.3:c.1675C>A XP_005267099.1:p.Pro559Thr
XM_011535920.1:c.1771C>A XP_011534222.1:p.Pro591Thr
XM_011535921.1:c.1657C>A XP_011534223.1:p.Pro553Thr
XM_011535922.1:c.1030C>A XP_011534224.1:p.Pro344Thr
XM_011535923.1:c.841C>A XP_011534225.1:p.Pro281Thr
XM_005267041.4:c.1771C>A XP_005267098.1:p.Pro591Thr
XM_005267042.4:c.1675C>A XP_005267099.1:p.Pro559Thr
XM_011535920.2:c.1771C>A XP_011534222.1:p.Pro591Thr
XM_011535921.2:c.1657C>A XP_011534223.1:p.Pro553Thr
XM_011535923.2:c.841C>A XP_011534225.1:p.Pro281Thr
XM_017010991.1:c.1171C>A XP_016866480.1:p.Pro391Thr
XM_017010992.1:c.1171C>A XP_016866481.1:p.Pro391Thr
XM_017010993.1:c.1171C>A XP_016866482.1:p.Pro391Thr
XM_017010994.1:c.1171C>A XP_016866483.1:p.Pro391Thr
NM_018013.4:c.1618C>A MANE Select NP_060483.3:p.Pro540Thr