Canonical Allele Identifier: CA397987772

Gene: HES7

Linked Data

• dbSNP Id: rs1981340739
• gnomAD v4: 17-8121750-C-T
• MyVariant Identifiers: chr17:g.8025068C>T (hg19) ; chr17:g.8121750C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121750C>T , CM000679.2:g.8121750C>T	GRCh38
NC_000017.10:g.8025068C>T , CM000679.1:g.8025068C>T	GRCh37
NC_000017.9:g.7965793C>T	NCBI36
NG_015807.1:g.2167G>A
NG_015816.1:g.7343G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.514G>A MANE Select	ENSP00000446205.2:p.Gly172Ser
ENST00000317814.8:c.499G>A	ENSP00000314774.4:p.Gly167Ser
ENST00000541682.6:c.514G>A	ENSP00000446205.2:p.Gly172Ser
NM_001165967.1:c.514G>A	NP_001159439.1:p.Gly172Ser
NM_032580.3:c.499G>A	NP_115969.2:p.Gly167Ser
XM_011524038.1:c.619G>A	XP_011522340.1:p.Gly207Ser
XM_011524039.1:c.610G>A	XP_011522341.1:p.Gly204Ser
XM_011524040.1:c.610G>A	XP_011522342.1:p.Gly204Ser
XM_011524041.1:c.601G>A	XP_011522343.1:p.Gly201Ser
XM_011524042.1:c.472G>A	XP_011522344.1:p.Gly158Ser
XR_934203.1:n.69+1936C>T
XM_017025232.1:c.619G>A	XP_016880721.1:p.Gly207Ser
XM_024451007.1:c.619G>A	XP_024306775.1:p.Gly207Ser
NM_001165967.2:c.514G>A MANE Select	NP_001159439.1:p.Gly172Ser
NM_032580.4:c.499G>A	NP_115969.2:p.Gly167Ser