Canonical Allele Identifier: CA1330172

Gene: GPR37L1

Linked Data

• dbSNP Id: rs763376779
• ExAC: 1:202097327 C / T
• gnomAD v2: 1-202097327-C-T
• gnomAD v4: 1-202128199-C-T
• MyVariant Identifiers: chr1:g.202097327C>T (hg19) ; chr1:g.202128199C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128199C>T , CM000663.2:g.202128199C>T	GRCh38
NC_000001.10:g.202097327C>T , CM000663.1:g.202097327C>T	GRCh37
NC_000001.9:g.200363950C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.705-35C>T
ENST00000682545.1:c.*95C>T	ENSP00000508402.1:n.*95C>T
ENST00000682887.1:c.1490C>T	ENSP00000506946.1:n.1490C>T
ENST00000683302.1:c.1020C>T	ENSP00000507885.1:p.Gly340=
ENST00000683557.1:c.715-35C>T	ENSP00000508029.1:n.715-35C>T
ENST00000367282.6:c.1089C>T MANE Select	ENSP00000356251.4:p.Gly363=
ENST00000367282.5:c.1089C>T	ENSP00000356251.4:p.Gly363=
NM_004767.3:c.1089C>T	NP_004758.3:p.Gly363=
XM_011510158.1:c.528C>T	XP_011508460.1:p.Gly176=
NM_004767.4:c.1089C>T	NP_004758.3:p.Gly363=
XM_011510158.2:c.528C>T	XP_011508460.1:p.Gly176=
NM_004767.5:c.1089C>T MANE Select	NP_004758.3:p.Gly363=