Canonical Allele Identifier: CA365170517

Gene: SOBP

Linked Data

• dbSNP Id: rs1231004766
• gnomAD v2: 6-107955681-C-T
• gnomAD v4: 6-107634477-C-T
• MyVariant Identifiers: chr6:g.107955681C>T (hg19) ; chr6:g.107634477C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634477C>T , CM000668.2:g.107634477C>T	GRCh38
NC_000006.11:g.107955681C>T , CM000668.1:g.107955681C>T	GRCh37
NC_000006.10:g.108062374C>T	NCBI36
NG_028200.1:g.149365C>T
NG_028200.2:g.149365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1633C>T MANE Select	ENSP00000318900.5:p.His545Tyr
ENST00000317357.9:c.1633C>T	ENSP00000318900.5:p.His545Tyr
NM_018013.3:c.1633C>T	NP_060483.3:p.His545Tyr
XM_005267041.3:c.1786C>T	XP_005267098.1:p.His596Tyr
XM_005267042.3:c.1690C>T	XP_005267099.1:p.His564Tyr
XM_011535920.1:c.1786C>T	XP_011534222.1:p.His596Tyr
XM_011535921.1:c.1672C>T	XP_011534223.1:p.His558Tyr
XM_011535922.1:c.1045C>T	XP_011534224.1:p.His349Tyr
XM_011535923.1:c.856C>T	XP_011534225.1:p.His286Tyr
XM_005267041.4:c.1786C>T	XP_005267098.1:p.His596Tyr
XM_005267042.4:c.1690C>T	XP_005267099.1:p.His564Tyr
XM_011535920.2:c.1786C>T	XP_011534222.1:p.His596Tyr
XM_011535921.2:c.1672C>T	XP_011534223.1:p.His558Tyr
XM_011535923.2:c.856C>T	XP_011534225.1:p.His286Tyr
XM_017010991.1:c.1186C>T	XP_016866480.1:p.His396Tyr
XM_017010992.1:c.1186C>T	XP_016866481.1:p.His396Tyr
XM_017010993.1:c.1186C>T	XP_016866482.1:p.His396Tyr
XM_017010994.1:c.1186C>T	XP_016866483.1:p.His396Tyr
NM_018013.4:c.1633C>T MANE Select	NP_060483.3:p.His545Tyr