Canonical Allele Identifier: CA365170933

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955735A>T (hg19) ; chr6:g.107634531A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634531A>T , CM000668.2:g.107634531A>T	GRCh38
NC_000006.11:g.107955735A>T , CM000668.1:g.107955735A>T	GRCh37
NC_000006.10:g.108062428A>T	NCBI36
NG_028200.1:g.149419A>T
NG_028200.2:g.149419A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1687A>T MANE Select	ENSP00000318900.5:p.Ile563Phe
ENST00000317357.9:c.1687A>T	ENSP00000318900.5:p.Ile563Phe
NM_018013.3:c.1687A>T	NP_060483.3:p.Ile563Phe
XM_005267041.3:c.1840A>T	XP_005267098.1:p.Ile614Phe
XM_005267042.3:c.1744A>T	XP_005267099.1:p.Ile582Phe
XM_011535920.1:c.1840A>T	XP_011534222.1:p.Ile614Phe
XM_011535921.1:c.1726A>T	XP_011534223.1:p.Ile576Phe
XM_011535922.1:c.1099A>T	XP_011534224.1:p.Ile367Phe
XM_011535923.1:c.910A>T	XP_011534225.1:p.Ile304Phe
XM_005267041.4:c.1840A>T	XP_005267098.1:p.Ile614Phe
XM_005267042.4:c.1744A>T	XP_005267099.1:p.Ile582Phe
XM_011535920.2:c.1840A>T	XP_011534222.1:p.Ile614Phe
XM_011535921.2:c.1726A>T	XP_011534223.1:p.Ile576Phe
XM_011535923.2:c.910A>T	XP_011534225.1:p.Ile304Phe
XM_017010991.1:c.1240A>T	XP_016866480.1:p.Ile414Phe
XM_017010992.1:c.1240A>T	XP_016866481.1:p.Ile414Phe
XM_017010993.1:c.1240A>T	XP_016866482.1:p.Ile414Phe
XM_017010994.1:c.1240A>T	XP_016866483.1:p.Ile414Phe
NM_018013.4:c.1687A>T MANE Select	NP_060483.3:p.Ile563Phe