Canonical Allele Identifier: CA365170786

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634508-T-A
• MyVariant Identifiers: chr6:g.107955712T>A (hg19) ; chr6:g.107634508T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634508T>A , CM000668.2:g.107634508T>A	GRCh38
NC_000006.11:g.107955712T>A , CM000668.1:g.107955712T>A	GRCh37
NC_000006.10:g.108062405T>A	NCBI36
NG_028200.1:g.149396T>A
NG_028200.2:g.149396T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1664T>A MANE Select	ENSP00000318900.5:p.Phe555Tyr
ENST00000317357.9:c.1664T>A	ENSP00000318900.5:p.Phe555Tyr
NM_018013.3:c.1664T>A	NP_060483.3:p.Phe555Tyr
XM_005267041.3:c.1817T>A	XP_005267098.1:p.Phe606Tyr
XM_005267042.3:c.1721T>A	XP_005267099.1:p.Phe574Tyr
XM_011535920.1:c.1817T>A	XP_011534222.1:p.Phe606Tyr
XM_011535921.1:c.1703T>A	XP_011534223.1:p.Phe568Tyr
XM_011535922.1:c.1076T>A	XP_011534224.1:p.Phe359Tyr
XM_011535923.1:c.887T>A	XP_011534225.1:p.Phe296Tyr
XM_005267041.4:c.1817T>A	XP_005267098.1:p.Phe606Tyr
XM_005267042.4:c.1721T>A	XP_005267099.1:p.Phe574Tyr
XM_011535920.2:c.1817T>A	XP_011534222.1:p.Phe606Tyr
XM_011535921.2:c.1703T>A	XP_011534223.1:p.Phe568Tyr
XM_011535923.2:c.887T>A	XP_011534225.1:p.Phe296Tyr
XM_017010991.1:c.1217T>A	XP_016866480.1:p.Phe406Tyr
XM_017010992.1:c.1217T>A	XP_016866481.1:p.Phe406Tyr
XM_017010993.1:c.1217T>A	XP_016866482.1:p.Phe406Tyr
XM_017010994.1:c.1217T>A	XP_016866483.1:p.Phe406Tyr
NM_018013.4:c.1664T>A MANE Select	NP_060483.3:p.Phe555Tyr