Canonical Allele Identifier: CA451581866

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955767G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634563G>C , CM000668.2:g.107634563G>C	GRCh38
NC_000006.11:g.107955767G>C , CM000668.1:g.107955767G>C	GRCh37
NC_000006.10:g.108062460G>C	NCBI36
NG_028200.1:g.149451G>C
NG_028200.2:g.149451G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1719G>C MANE Select	ENSP00000318900.5:p.Ala573=
ENST00000317357.9:c.1719G>C	ENSP00000318900.5:p.Ala573=
NM_018013.3:c.1719G>C	NP_060483.3:p.Ala573=
XM_005267041.3:c.1872G>C	XP_005267098.1:p.Ala624=
XM_005267042.3:c.1776G>C	XP_005267099.1:p.Ala592=
XM_011535920.1:c.1872G>C	XP_011534222.1:p.Ala624=
XM_011535921.1:c.1758G>C	XP_011534223.1:p.Ala586=
XM_011535922.1:c.1131G>C	XP_011534224.1:p.Ala377=
XM_011535923.1:c.942G>C	XP_011534225.1:p.Ala314=
XM_005267041.4:c.1872G>C	XP_005267098.1:p.Ala624=
XM_005267042.4:c.1776G>C	XP_005267099.1:p.Ala592=
XM_011535920.2:c.1872G>C	XP_011534222.1:p.Ala624=
XM_011535921.2:c.1758G>C	XP_011534223.1:p.Ala586=
XM_011535923.2:c.942G>C	XP_011534225.1:p.Ala314=
XM_017010991.1:c.1272G>C	XP_016866480.1:p.Ala424=
XM_017010992.1:c.1272G>C	XP_016866481.1:p.Ala424=
XM_017010993.1:c.1272G>C	XP_016866482.1:p.Ala424=
XM_017010994.1:c.1272G>C	XP_016866483.1:p.Ala424=
NM_018013.4:c.1719G>C MANE Select	NP_060483.3:p.Ala573=