Canonical Allele Identifier: CA451581903

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955779A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634575A>C , CM000668.2:g.107634575A>C	GRCh38
NC_000006.11:g.107955779A>C , CM000668.1:g.107955779A>C	GRCh37
NC_000006.10:g.108062472A>C	NCBI36
NG_028200.1:g.149463A>C
NG_028200.2:g.149463A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1731A>C MANE Select	ENSP00000318900.5:p.Pro577=
ENST00000317357.9:c.1731A>C	ENSP00000318900.5:p.Pro577=
NM_018013.3:c.1731A>C	NP_060483.3:p.Pro577=
XM_005267041.3:c.1884A>C	XP_005267098.1:p.Pro628=
XM_005267042.3:c.1788A>C	XP_005267099.1:p.Pro596=
XM_011535920.1:c.1884A>C	XP_011534222.1:p.Pro628=
XM_011535921.1:c.1770A>C	XP_011534223.1:p.Pro590=
XM_011535922.1:c.1143A>C	XP_011534224.1:p.Pro381=
XM_011535923.1:c.954A>C	XP_011534225.1:p.Pro318=
XM_005267041.4:c.1884A>C	XP_005267098.1:p.Pro628=
XM_005267042.4:c.1788A>C	XP_005267099.1:p.Pro596=
XM_011535920.2:c.1884A>C	XP_011534222.1:p.Pro628=
XM_011535921.2:c.1770A>C	XP_011534223.1:p.Pro590=
XM_011535923.2:c.954A>C	XP_011534225.1:p.Pro318=
XM_017010991.1:c.1284A>C	XP_016866480.1:p.Pro428=
XM_017010992.1:c.1284A>C	XP_016866481.1:p.Pro428=
XM_017010993.1:c.1284A>C	XP_016866482.1:p.Pro428=
XM_017010994.1:c.1284A>C	XP_016866483.1:p.Pro428=
NM_018013.4:c.1731A>C MANE Select	NP_060483.3:p.Pro577=