Canonical Allele Identifier: CA3946561
Gene: SOBP HGNC NCBI

Linked Data

dbSNP Id: rs753882086

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634526A>T , CM000668.2:g.107634526A>T GRCh38
NC_000006.11:g.107955730A>T , CM000668.1:g.107955730A>T GRCh37
NC_000006.10:g.108062423A>T NCBI36
NG_028200.1:g.149414A>T
NG_028200.2:g.149414A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1682A>T MANE Select ENSP00000318900.5:p.Asn561Ile
ENST00000317357.9:c.1682A>T ENSP00000318900.5:p.Asn561Ile
NM_018013.3:c.1682A>T NP_060483.3:p.Asn561Ile
XM_005267041.3:c.1835A>T XP_005267098.1:p.Asn612Ile
XM_005267042.3:c.1739A>T XP_005267099.1:p.Asn580Ile
XM_011535920.1:c.1835A>T XP_011534222.1:p.Asn612Ile
XM_011535921.1:c.1721A>T XP_011534223.1:p.Asn574Ile
XM_011535922.1:c.1094A>T XP_011534224.1:p.Asn365Ile
XM_011535923.1:c.905A>T XP_011534225.1:p.Asn302Ile
XM_005267041.4:c.1835A>T XP_005267098.1:p.Asn612Ile
XM_005267042.4:c.1739A>T XP_005267099.1:p.Asn580Ile
XM_011535920.2:c.1835A>T XP_011534222.1:p.Asn612Ile
XM_011535921.2:c.1721A>T XP_011534223.1:p.Asn574Ile
XM_011535923.2:c.905A>T XP_011534225.1:p.Asn302Ile
XM_017010991.1:c.1235A>T XP_016866480.1:p.Asn412Ile
XM_017010992.1:c.1235A>T XP_016866481.1:p.Asn412Ile
XM_017010993.1:c.1235A>T XP_016866482.1:p.Asn412Ile
XM_017010994.1:c.1235A>T XP_016866483.1:p.Asn412Ile
NM_018013.4:c.1682A>T MANE Select NP_060483.3:p.Asn561Ile