Canonical Allele Identifier: CA365170897

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955729A>T (hg19) ; chr6:g.107634525A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634525A>T , CM000668.2:g.107634525A>T	GRCh38
NC_000006.11:g.107955729A>T , CM000668.1:g.107955729A>T	GRCh37
NC_000006.10:g.108062422A>T	NCBI36
NG_028200.1:g.149413A>T
NG_028200.2:g.149413A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1681A>T MANE Select	ENSP00000318900.5:p.Asn561Tyr
ENST00000317357.9:c.1681A>T	ENSP00000318900.5:p.Asn561Tyr
NM_018013.3:c.1681A>T	NP_060483.3:p.Asn561Tyr
XM_005267041.3:c.1834A>T	XP_005267098.1:p.Asn612Tyr
XM_005267042.3:c.1738A>T	XP_005267099.1:p.Asn580Tyr
XM_011535920.1:c.1834A>T	XP_011534222.1:p.Asn612Tyr
XM_011535921.1:c.1720A>T	XP_011534223.1:p.Asn574Tyr
XM_011535922.1:c.1093A>T	XP_011534224.1:p.Asn365Tyr
XM_011535923.1:c.904A>T	XP_011534225.1:p.Asn302Tyr
XM_005267041.4:c.1834A>T	XP_005267098.1:p.Asn612Tyr
XM_005267042.4:c.1738A>T	XP_005267099.1:p.Asn580Tyr
XM_011535920.2:c.1834A>T	XP_011534222.1:p.Asn612Tyr
XM_011535921.2:c.1720A>T	XP_011534223.1:p.Asn574Tyr
XM_011535923.2:c.904A>T	XP_011534225.1:p.Asn302Tyr
XM_017010991.1:c.1234A>T	XP_016866480.1:p.Asn412Tyr
XM_017010992.1:c.1234A>T	XP_016866481.1:p.Asn412Tyr
XM_017010993.1:c.1234A>T	XP_016866482.1:p.Asn412Tyr
XM_017010994.1:c.1234A>T	XP_016866483.1:p.Asn412Tyr
NM_018013.4:c.1681A>T MANE Select	NP_060483.3:p.Asn561Tyr